|
Q9HA33
|
APID
|
UniProt
|
KSYTTPCMVTG
|
12-22
|
11.87
|
nd
|
nd
|
nd
|
nd
|
Q9HA33_HUMAN cDNA FLJ12331 fis, clone MAMMA1002170, moderately similar to 40S RIBOSOMAL PROTEIN S2 - Homo sapiens
|
|
Q9ULL1
|
APID
|
UniProt
|
DSDKLNDYLWR
|
1349-1359
|
11.87
|
nd
|
nd
|
nd
|
nd
|
PKHG1_HUMAN Pleckstrin homology domain-containing family G member 1 - Homo sapiens
|
|
Q2M3Q8
|
APID
|
UniProt
|
KSYTTPCMVTG
|
12-22
|
11.87
|
nd
|
nd
|
nd
|
nd
|
Q2M3Q8_HUMAN Ribosomal protein S2 pseudogene - Homo sapiens
|
|
Q5TIG5
|
APID
|
UniProt
|
EGFELYNNSTQ
|
1127-1137
|
11.87
|
nd
|
nd
|
nd
|
nd
|
Q5TIG5_HUMAN Myeloid/lymphoid or mixed-lineage leukemia (Trithorax homolog, Drosophila); translocated to, 4 - Homo sapiens
|
|
A2RUN2
|
APID
|
UniProt
|
PTSSKDNYLGG
|
216-226
|
11.87
|
nd
|
nd
|
nd
|
nd
|
A2RUN2_HUMAN AR protein - Homo sapiens
|
|
A8MQ02
|
APID
|
UniProt
|
EGFELYNNSTQ
|
1127-1137
|
11.87
|
nd
|
nd
|
nd
|
nd
|
A8MQ02_HUMAN Uncharacterized protein MLLT4 - Homo sapiens
|
|
Q9BS19
|
APID
|
UniProt
|
VPPRYPRDVRD
|
216-226
|
11.88
|
nd
|
nd
|
nd
|
nd
|
Q9BS19_HUMAN HPX protein - Homo sapiens
|
|
Q5VYK7
|
APID
|
UniProt
|
DYRENHNNNKK
|
102-112
|
11.88
|
nd
|
nd
|
nd
|
nd
|
Q5VYK7_HUMAN G patch domain containing 2 - Homo sapiens
|
|
Q5VYK8
|
APID
|
UniProt
|
DYRENHNNNKK
|
102-112
|
11.88
|
nd
|
nd
|
nd
|
nd
|
Q5VYK8_HUMAN G patch domain containing 2 - Homo sapiens
|
|
A8K3U1
|
APID
|
UniProt
|
GRSSKYGLLHC
|
262-272
|
11.88
|
nd
|
nd
|
nd
|
nd
|
A8K3U1_HUMAN cDNA FLJ78403, highly similar to Homo sapiens SLAM family member 7, mRNA - Homo sapiens
|
|
Q4KKW9
|
APID
|
UniProt
|
PDSSFYKGLDL
|
354-364
|
11.88
|
nd
|
nd
|
nd
|
nd
|
Q4KKW9_HUMAN Solute carrier family 4, anion exchanger, member 1 - Homo sapiens
|
|
Q5VZL5
|
APID
|
UniProt
|
LTPTLDSMSYG
|
45-55
|
11.88
|
nd
|
nd
|
nd
|
nd
|
ZMYM4_HUMAN Zinc finger MYM-type protein 4 - Homo sapiens
|
|
Q99504
|
APID
|
UniProt
|
NLNNYSFSTNG
|
379-389
|
11.88
|
nd
|
nd
|
nd
|
nd
|
EYA3_HUMAN Eyes absent homolog 3 - Homo sapiens
|
|
A8K5C3
|
APID
|
UniProt
|
DYRENHNNNKK
|
102-112
|
11.88
|
nd
|
nd
|
nd
|
nd
|
A8K5C3_HUMAN cDNA FLJ77283, highly similar to Homo sapiens G patch domain containing 2, mRNA - Homo sapiens
|
|
A8K114
|
APID
|
UniProt
|
SNLQGPYLASG
|
441-451
|
11.88
|
nd
|
nd
|
nd
|
nd
|
A8K114_HUMAN cDNA FLJ77009, highly similar to Homo sapiens calcium channel, voltage-dependent, beta 1 subunit (CACNB1), transcript variant 1, mRNA - Homo sapiens
|
|
Q9NW75
|
APID
|
UniProt
|
DYRENHNNNKK
|
102-112
|
11.88
|
nd
|
nd
|
nd
|
nd
|
GPTC2_HUMAN G patch domain-containing protein 2 - Homo sapiens
|
|
A0T124
|
APID
|
UniProt
|
PLPEYCNPEGK
|
2104-2114
|
11.88
|
nd
|
nd
|
nd
|
nd
|
A0T124_HUMAN Jumonji domain-containing 1 C splice variant - Homo sapiens
|
|
A6PW35
|
APID
|
UniProt
|
PLPEYCNPEGK
|
1827-1837
|
11.88
|
nd
|
nd
|
nd
|
nd
|
A6PW35_HUMAN Jumonji domain containing 1C - Homo sapiens
|
|
Q02641
|
APID
|
UniProt
|
SNLQGPYLASG
|
441-451
|
11.88
|
nd
|
nd
|
nd
|
nd
|
CACB1_HUMAN Voltage-dependent L-type calcium channel subunit beta-1 - Homo sapiens
|
|
Q1ZZ45
|
APID
|
UniProt
|
PDSSFYKGLDL
|
354-364
|
11.88
|
nd
|
nd
|
nd
|
nd
|
Q1ZZ45_HUMAN Solute carrier family 4 anion exchanger member 1 variant - Homo sapiens
|