|
O75086
|
APID
|
UniProt
|
PQERESVLV
|
349-357
|
7.17
|
nd
|
nd
|
nd
|
nd
|
O75086_HUMAN MIFR-2 - Homo sapiens
|
|
A8K3H9
|
APID
|
UniProt
|
GDGGTASLV
|
545-553
|
7.17
|
nd
|
nd
|
nd
|
nd
|
A8K3H9_HUMAN cDNA FLJ75649, highly similar to Homo sapiens v-rel reticuloendotheliosis viral oncogene homolog B, nuclear factor of kappa light polypeptide gene enhancer in B-cells 3 - Homo sapiens
|
|
Q5VVX3
|
APID
|
UniProt
|
PCPRCHVPV
|
268-276
|
7.18
|
nd
|
nd
|
nd
|
nd
|
Q5VVX3_HUMAN Parkinson disease (Autosomal recessive, juvenile) 2, parkin - Homo sapiens
|
|
Q9P206
|
APID
|
UniProt
|
PPEEAFFSV
|
730-738
|
7.18
|
nd
|
nd
|
nd
|
nd
|
K1522_HUMAN Uncharacterized protein KIAA1522 - Homo sapiens
|
|
A1IGZ9
|
APID
|
UniProt
|
PCPRCHVPV
|
417-425
|
7.18
|
nd
|
nd
|
nd
|
nd
|
A1IGZ9_HUMAN Parkin 2 - Homo sapiens
|
|
Q6ZSM9
|
APID
|
UniProt
|
LLDKDDLAI
|
58-66
|
7.18
|
nd
|
nd
|
nd
|
nd
|
Q6ZSM9_HUMAN cDNA FLJ45358 fis, clone BRHIP3013078, moderately similar to Homo sapiens BAI1-associated protein 2 - Homo sapiens
|
|
Q92615
|
APID
|
UniProt
|
PADMNALAL
|
121-129
|
7.18
|
nd
|
nd
|
nd
|
nd
|
LARP5_HUMAN La-related protein 5 - Homo sapiens
|
|
Q6PFW2
|
APID
|
UniProt
|
PEDGSDAPL
|
1541-1549
|
7.18
|
nd
|
nd
|
nd
|
nd
|
Q6PFW2_HUMAN Rho guanine nucleotide exchange factor (GEF) 11 - Homo sapiens
|
|
A8K1T0
|
APID
|
UniProt
|
NFSYGDYDL
|
27-35
|
7.18
|
nd
|
nd
|
nd
|
nd
|
A8K1T0_HUMAN cDNA FLJ76003, highly similar to Homo sapiens G protein-coupled receptor 73-like 1 (GPR73L1), mRNA - Homo sapiens
|
|
A5JUU1
|
APID
|
UniProt
|
NFSYGDYDL
|
27-35
|
7.18
|
nd
|
nd
|
nd
|
nd
|
A5JUU1_HUMAN Prokineticin receptor 2 - Homo sapiens
|
|
A8K975
|
APID
|
UniProt
|
PCPRCHVPV
|
417-425
|
7.18
|
nd
|
nd
|
nd
|
nd
|
A8K975_HUMAN cDNA FLJ75810, highly similar to Homo sapiens Parkinson disease (autosomal recessive, juvenile) 2, parkin (PARK2), transcript variant 1, mRNA - Homo sapiens
|
|
A7MD20
|
APID
|
UniProt
|
PADMNALAL
|
121-129
|
7.18
|
nd
|
nd
|
nd
|
nd
|
A7MD20_HUMAN La ribonucleoprotein domain family, member 5 - Homo sapiens
|
|
Q9H880
|
APID
|
UniProt
|
PNWSANFDV
|
9-17
|
7.18
|
nd
|
nd
|
nd
|
nd
|
Q9H880_HUMAN cDNA FLJ13888 fis, clone THYRO1001584 - Homo sapiens
|
|
Q5SZW4
|
APID
|
UniProt
|
GLGGLLLKL
|
340-348
|
7.18
|
nd
|
nd
|
nd
|
nd
|
Q5SZW4_HUMAN Rh family, B glycoprotein - Homo sapiens
|
|
Q5VVX4
|
APID
|
UniProt
|
PCPRCHVPV
|
389-397
|
7.18
|
nd
|
nd
|
nd
|
nd
|
Q5VVX4_HUMAN Parkinson disease (Autosomal recessive, juvenile) 2, parkin - Homo sapiens
|
|
Q5JQ23
|
APID
|
UniProt
|
QIDNMDSNV
|
740-748
|
7.18
|
nd
|
nd
|
nd
|
nd
|
Q5JQ23_HUMAN Potassium large conductance calcium-activated channel, subfamily M, alpha member 1 - Homo sapiens
|
|
Q6GSG7
|
APID
|
UniProt
|
YYNSPGLHV
|
392-400
|
7.18
|
nd
|
nd
|
nd
|
nd
|
Q6GSG7_HUMAN Coiled-coil domain containing 6 - Homo sapiens
|
|
Q6PQD3
|
APID
|
UniProt
|
HMTSMYLPL
|
43-51
|
7.18
|
nd
|
nd
|
nd
|
nd
|
Q6PQD3_HUMAN Helios 1+2b,2c isoform - Homo sapiens
|
|
Q5VVX1
|
APID
|
UniProt
|
PCPRCHVPV
|
226-234
|
7.18
|
nd
|
nd
|
nd
|
nd
|
Q5VVX1_HUMAN Parkinson disease (Autosomal recessive, juvenile) 2, parkin - Homo sapiens
|
|
A6NEL6
|
APID
|
UniProt
|
PADMNALAL
|
121-129
|
7.18
|
nd
|
nd
|
nd
|
nd
|
A6NEL6_HUMAN Uncharacterized protein LARP5 - Homo sapiens
|
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