|
Q5T200
|
APID
|
UniProt
|
QKRSSSLGSNR
|
1186-1196
|
16.98
|
nd
|
nd
|
nd
|
nd
|
ZC3HD_HUMAN Zinc finger CCCH domain-containing protein 13 - Homo sapiens
|
|
A6NKC6
|
APID
|
UniProt
|
PQRRSSSCGST
|
863-873
|
16.98
|
nd
|
nd
|
nd
|
nd
|
A6NKC6_HUMAN Uncharacterized protein RP1L1 - Homo sapiens
|
|
Q8IWN7
|
APID
|
UniProt
|
PQRRSSSCGST
|
863-873
|
16.98
|
nd
|
nd
|
nd
|
nd
|
RP1L1_HUMAN Retinitis pigmentosa 1-like 1 protein - Homo sapiens
|
|
Q6PJ65
|
APID
|
UniProt
|
HRPPTSGCLGP
|
23-33
|
16.98
|
nd
|
nd
|
nd
|
nd
|
Q6PJ65_HUMAN TSPAN10 protein - Homo sapiens
|
|
Q8N8E5
|
APID
|
UniProt
|
HRPPTSGCLGP
|
23-33
|
16.98
|
nd
|
nd
|
nd
|
nd
|
Q8N8E5_HUMAN cDNA FLJ39607 fis, clone SKNSH2006304, weakly similar to Homo sapiens tetraspan NET-4 mRNA - Homo sapiens
|
|
Q68DI8
|
APID
|
UniProt
|
ILGGSRQPSSP
|
126-136
|
16.98
|
nd
|
nd
|
nd
|
nd
|
Q68DI8_HUMAN Putative uncharacterized protein DKFZp781B109 - Homo sapiens
|
|
Q19R11
|
APID
|
UniProt
|
RRTSSSGSAEP
|
1044-1054
|
17.26
|
nd
|
nd
|
nd
|
nd
|
Q19R11_HUMAN T calcium channel alpha 1G subunit variant 93 - Homo sapiens
|
|
Q19R15
|
APID
|
UniProt
|
RRTSSSGSAEP
|
1044-1054
|
17.26
|
nd
|
nd
|
nd
|
nd
|
Q19R15_HUMAN T calcium channel alpha 1G subunit variant 49 - Homo sapiens
|
|
Q19R16
|
APID
|
UniProt
|
RRTSSSGSAEP
|
1044-1054
|
17.26
|
nd
|
nd
|
nd
|
nd
|
Q19R16_HUMAN T calcium channel alpha 1G subunit variant 33 - Homo sapiens
|
|
Q19QY9
|
APID
|
UniProt
|
RRTSSSGSAEP
|
1067-1077
|
17.26
|
nd
|
nd
|
nd
|
nd
|
Q19QY9_HUMAN T calcium channel alpha 1G subunit variant 473-d81 - Homo sapiens
|
|
Q19R06
|
APID
|
UniProt
|
RRTSSSGSAEP
|
1067-1077
|
17.26
|
nd
|
nd
|
nd
|
nd
|
Q19R06_HUMAN T calcium channel alpha 1G subunit variant 169 - Homo sapiens
|
|
Q19R07
|
APID
|
UniProt
|
RRTSSSGSAEP
|
1067-1077
|
17.26
|
nd
|
nd
|
nd
|
nd
|
Q19R07_HUMAN T calcium channel alpha 1G subunit variant 157 - Homo sapiens
|
|
Q19QZ8
|
APID
|
UniProt
|
RRTSSSGSAEP
|
1067-1077
|
17.26
|
nd
|
nd
|
nd
|
nd
|
Q19QZ8_HUMAN T calcium channel alpha 1G subunit variant 221 - Homo sapiens
|
|
Q19R00
|
APID
|
UniProt
|
RRTSSSGSAEP
|
1067-1077
|
17.26
|
nd
|
nd
|
nd
|
nd
|
Q19R00_HUMAN T calcium channel alpha 1G subunit variant 216 - Homo sapiens
|
|
A8K488
|
APID
|
UniProt
|
SSRFSSGGACG
|
53-63
|
17.26
|
nd
|
nd
|
nd
|
nd
|
A8K488_HUMAN cDNA FLJ75925, highly similar to Homo sapiens keratin 16 - Homo sapiens
|
|
Q19R08
|
APID
|
UniProt
|
RRTSSSGSAEP
|
1067-1077
|
17.26
|
nd
|
nd
|
nd
|
nd
|
Q19R08_HUMAN T calcium channel alpha 1G subunit variant 153 - Homo sapiens
|
|
Q19R01
|
APID
|
UniProt
|
RRTSSSGSAEP
|
1067-1077
|
17.26
|
nd
|
nd
|
nd
|
nd
|
Q19R01_HUMAN T calcium channel alpha 1G subunit variant 209 - Homo sapiens
|
|
Q19R05
|
APID
|
UniProt
|
RRTSSSGSAEP
|
1067-1077
|
17.26
|
nd
|
nd
|
nd
|
nd
|
Q19R05_HUMAN T calcium channel alpha 1G subunit variant 177 - Homo sapiens
|
|
Q52M62
|
APID
|
UniProt
|
RSRPGSCPSAS
|
38-48
|
17.26
|
nd
|
nd
|
nd
|
nd
|
Q52M62_HUMAN LOC285908 protein - Homo sapiens
|
|
Q19R10
|
APID
|
UniProt
|
RRTSSSGSAEP
|
1067-1077
|
17.26
|
nd
|
nd
|
nd
|
nd
|
Q19R10_HUMAN T calcium channel alpha 1G subunit variant 137 - Homo sapiens
|