Q7Z6Q1
|
APID
|
UniProt
|
PRPPSNPPARGTLK
|
379-392
|
22.55
|
nd
|
nd
|
nd
|
nd
|
Q7Z6Q1_HUMAN TRAF3 interacting protein 2 - Homo sapiens
|
A6H8X7
|
APID
|
UniProt
|
GSGRSQSNGVLATE
|
486-499
|
22.55
|
nd
|
nd
|
nd
|
nd
|
A6H8X7_HUMAN Jumonji domain containing 1B - Homo sapiens
|
Q7LBC6
|
APID
|
UniProt
|
GSGRSQSNGVLATE
|
486-499
|
22.55
|
nd
|
nd
|
nd
|
nd
|
JHD2B_HUMAN JmjC domain-containing histone demethylation protein 2B - Homo sapiens
|
O43734
|
APID
|
UniProt
|
PRPPSNPPARGTLK
|
388-401
|
22.55
|
nd
|
nd
|
nd
|
nd
|
CIKS_HUMAN Adapter protein CIKS - Homo sapiens
|
Q5VZP5
|
APID
|
UniProt
|
PQDGGGWRSASSGQ
|
366-379
|
22.55
|
nd
|
nd
|
nd
|
nd
|
DUS27_HUMAN Inactive dual specificity phosphatase 27 - Homo sapiens
|
Q5QTR7
|
APID
|
UniProt
|
GRPSRTSSSGSSSS
|
68-81
|
22.56
|
nd
|
nd
|
nd
|
nd
|
Q5QTR7_HUMAN FWP009 - Homo sapiens
|
Q8WXS5
|
APID
|
UniProt
|
AERDRGGSSGFLTL
|
355-368
|
22.56
|
nd
|
nd
|
nd
|
nd
|
CCG8_HUMAN Voltage-dependent calcium channel gamma-8 subunit - Homo sapiens
|
A8K064
|
APID
|
UniProt
|
SNFRGGSDGYGSGR
|
225-238
|
22.56
|
nd
|
nd
|
nd
|
nd
|
A8K064_HUMAN cDNA FLJ75945, highly similar to Homo sapiens heterogeneous nuclear ribonucleoprotein A2/B1 (HNRPA2B1), transcript variant B1, mRNA - Homo sapiens
|
P22626
|
APID
|
UniProt
|
SNFRGGSDGYGSGR
|
225-238
|
22.56
|
nd
|
nd
|
nd
|
nd
|
ROA2_HUMAN Heterogeneous nuclear ribonucleoproteins A2/B1 - Homo sapiens
|
P08047
|
APID
|
UniProt
|
GAFSQARSSSTGSS
|
33-46
|
22.56
|
nd
|
nd
|
nd
|
nd
|
SP1_HUMAN Transcription factor Sp1 - Homo sapiens
|
Q5THK1
|
APID
|
UniProt
|
SPHCKRQPSLGTTS
|
1905-1918
|
22.57
|
nd
|
nd
|
nd
|
nd
|
CV030_HUMAN Uncharacterized protein C22orf30 - Homo sapiens
|
Q5BQ95
|
APID
|
UniProt
|
PHCRTLSKGGAQSL
|
73-86
|
22.57
|
nd
|
nd
|
nd
|
nd
|
Q5BQ95_HUMAN Kallikrein 13 splice variant 8 - Homo sapiens
|
O95678
|
APID
|
UniProt
|
LSSGYGRGSSIGGG
|
479-492
|
22.57
|
nd
|
nd
|
nd
|
nd
|
K2C75_HUMAN Keratin, type II cytoskeletal 75 - Homo sapiens
|
Q19QZ9
|
APID
|
UniProt
|
GPASRRTSSSGSAE
|
1063-1076
|
22.58
|
nd
|
nd
|
nd
|
nd
|
Q19QZ9_HUMAN T calcium channel alpha 1G subunit variant 217 - Homo sapiens
|
Q19R17
|
APID
|
UniProt
|
GPASRRTSSSGSAE
|
1040-1053
|
22.58
|
nd
|
nd
|
nd
|
nd
|
Q19R17_HUMAN T calcium channel alpha 1G subunit variant 25 - Homo sapiens
|
Q19R13
|
APID
|
UniProt
|
GPASRRTSSSGSAE
|
1040-1053
|
22.58
|
nd
|
nd
|
nd
|
nd
|
Q19R13_HUMAN T calcium channel alpha 1G subunit variant 88 - Homo sapiens
|
Q19QY8
|
APID
|
UniProt
|
GPASRRTSSSGSAE
|
1063-1076
|
22.58
|
nd
|
nd
|
nd
|
nd
|
Q19QY8_HUMAN T calcium channel alpha 1G subunit variant 477 - Homo sapiens
|
Q19R09
|
APID
|
UniProt
|
GPASRRTSSSGSAE
|
1063-1076
|
22.58
|
nd
|
nd
|
nd
|
nd
|
Q19R09_HUMAN T calcium channel alpha 1G subunit variant 145 - Homo sapiens
|
Q19R05
|
APID
|
UniProt
|
GPASRRTSSSGSAE
|
1063-1076
|
22.58
|
nd
|
nd
|
nd
|
nd
|
Q19R05_HUMAN T calcium channel alpha 1G subunit variant 177 - Homo sapiens
|
Q19QY9
|
APID
|
UniProt
|
GPASRRTSSSGSAE
|
1063-1076
|
22.58
|
nd
|
nd
|
nd
|
nd
|
Q19QY9_HUMAN T calcium channel alpha 1G subunit variant 473-d81 - Homo sapiens
|