|
Q19R02
|
APID
|
UniProt
|
SLPNDSYMCRH
|
2001-2011
|
11.86
|
nd
|
nd
|
nd
|
nd
|
Q19R02_HUMAN T calcium channel alpha 1G subunit variant 189 - Homo sapiens
|
|
Q19R03
|
APID
|
UniProt
|
SLPNDSYMCRH
|
1953-1963
|
11.86
|
nd
|
nd
|
nd
|
nd
|
Q19R03_HUMAN T calcium channel alpha 1G subunit variant 185 - Homo sapiens
|
|
Q19QZ9
|
APID
|
UniProt
|
SLPNDSYMCRH
|
1942-1952
|
11.86
|
nd
|
nd
|
nd
|
nd
|
Q19QZ9_HUMAN T calcium channel alpha 1G subunit variant 217 - Homo sapiens
|
|
Q5SQL3
|
APID
|
UniProt
|
YTFQHGSPLHS
|
1037-1047
|
11.86
|
nd
|
nd
|
nd
|
nd
|
Q5SQL3_HUMAN Homeodomain interacting protein kinase 1 - Homo sapiens
|
|
Q19R00
|
APID
|
UniProt
|
SLPNDSYMCRH
|
1942-1952
|
11.86
|
nd
|
nd
|
nd
|
nd
|
Q19R00_HUMAN T calcium channel alpha 1G subunit variant 216 - Homo sapiens
|
|
Q19R06
|
APID
|
UniProt
|
SLPNDSYMCRH
|
1946-1956
|
11.86
|
nd
|
nd
|
nd
|
nd
|
Q19R06_HUMAN T calcium channel alpha 1G subunit variant 169 - Homo sapiens
|
|
Q49A68
|
APID
|
UniProt
|
PVKLRTYLGDP
|
38-48
|
11.86
|
nd
|
nd
|
nd
|
nd
|
Q49A68_HUMAN TMEM68 protein - Homo sapiens
|
|
Q8N637
|
APID
|
UniProt
|
GDSLPYHQLQG
|
23-33
|
11.86
|
nd
|
nd
|
nd
|
nd
|
Q8N637_HUMAN Down syndrome critical region gene 9 - Homo sapiens
|
|
Q96MH6
|
APID
|
UniProt
|
PVKLRTYLGDP
|
271-281
|
11.86
|
nd
|
nd
|
nd
|
nd
|
TMM68_HUMAN Transmembrane protein 68 - Homo sapiens
|
|
P59020
|
APID
|
UniProt
|
GDSLPYHQLQG
|
23-33
|
11.86
|
nd
|
nd
|
nd
|
nd
|
DSCR9_HUMAN Down syndrome critical region protein 9 - Homo sapiens
|
|
Q86YZ3
|
APID
|
UniProt
|
ENDSYSRNVRG
|
136-146
|
11.86
|
nd
|
nd
|
nd
|
nd
|
HORN_HUMAN Hornerin - Homo sapiens
|
|
Q19R07
|
APID
|
UniProt
|
SLPNDSYMCRH
|
1983-1993
|
11.86
|
nd
|
nd
|
nd
|
nd
|
Q19R07_HUMAN T calcium channel alpha 1G subunit variant 157 - Homo sapiens
|
|
Q6NWT2
|
APID
|
UniProt
|
TVFKYDRFLNP
|
401-411
|
11.86
|
nd
|
nd
|
nd
|
nd
|
Q6NWT2_HUMAN Cytochrome P450, family 8, subfamily B, polypeptide 1 - Homo sapiens
|
|
Q19QZ8
|
APID
|
UniProt
|
SLPNDSYMCRH
|
1990-2000
|
11.86
|
nd
|
nd
|
nd
|
nd
|
Q19QZ8_HUMAN T calcium channel alpha 1G subunit variant 221 - Homo sapiens
|
|
A6ND53
|
APID
|
UniProt
|
YPHTQGDFSFD
|
178-188
|
11.86
|
nd
|
nd
|
nd
|
nd
|
A6ND53_HUMAN Uncharacterized protein MKL2 - Homo sapiens
|
|
Q19QZ3
|
APID
|
UniProt
|
SLPNDSYMCRH
|
1919-1929
|
11.86
|
nd
|
nd
|
nd
|
nd
|
Q19QZ3_HUMAN T calcium channel alpha 1G subunit variant 441 - Homo sapiens
|
|
Q9ULH7
|
APID
|
UniProt
|
YPHTQGDFSFD
|
167-177
|
11.86
|
nd
|
nd
|
nd
|
nd
|
MKL2_HUMAN MKL/myocardin-like protein 2 - Homo sapiens
|
|
Q19QZ6
|
APID
|
UniProt
|
SLPNDSYMCRH
|
1960-1970
|
11.86
|
nd
|
nd
|
nd
|
nd
|
Q19QZ6_HUMAN T calcium channel alpha 1G subunit variant 249 - Homo sapiens
|
|
Q5U1F4
|
APID
|
UniProt
|
ENDSYSRNVRG
|
136-146
|
11.86
|
nd
|
nd
|
nd
|
nd
|
Q5U1F4_HUMAN Hornerin - Homo sapiens
|
|
Q19R10
|
APID
|
UniProt
|
SLPNDSYMCRH
|
1928-1938
|
11.86
|
nd
|
nd
|
nd
|
nd
|
Q19R10_HUMAN T calcium channel alpha 1G subunit variant 137 - Homo sapiens
|