Q19R04
|
APID
|
UniProt
|
SRTHSLPNDSY
|
1949-1959
|
13.49
|
nd
|
nd
|
nd
|
nd
|
Q19R04_HUMAN T calcium channel alpha 1G subunit variant 184 - Homo sapiens
|
Q19R12
|
APID
|
UniProt
|
SRTHSLPNDSY
|
1915-1925
|
13.49
|
nd
|
nd
|
nd
|
nd
|
Q19R12_HUMAN T calcium channel alpha 1G subunit variant 89 - Homo sapiens
|
Q19R03
|
APID
|
UniProt
|
SRTHSLPNDSY
|
1949-1959
|
13.49
|
nd
|
nd
|
nd
|
nd
|
Q19R03_HUMAN T calcium channel alpha 1G subunit variant 185 - Homo sapiens
|
Q19R13
|
APID
|
UniProt
|
SRTHSLPNDSY
|
1915-1925
|
13.49
|
nd
|
nd
|
nd
|
nd
|
Q19R13_HUMAN T calcium channel alpha 1G subunit variant 88 - Homo sapiens
|
Q19R17
|
APID
|
UniProt
|
SRTHSLPNDSY
|
1908-1918
|
13.49
|
nd
|
nd
|
nd
|
nd
|
Q19R17_HUMAN T calcium channel alpha 1G subunit variant 25 - Homo sapiens
|
Q19QZ5
|
APID
|
UniProt
|
SRTHSLPNDSY
|
1892-1902
|
13.49
|
nd
|
nd
|
nd
|
nd
|
Q19QZ5_HUMAN T calcium channel alpha 1G subunit variant 313 - Homo sapiens
|
Q19R07
|
APID
|
UniProt
|
SRTHSLPNDSY
|
1979-1989
|
13.49
|
nd
|
nd
|
nd
|
nd
|
Q19R07_HUMAN T calcium channel alpha 1G subunit variant 157 - Homo sapiens
|
Q19R08
|
APID
|
UniProt
|
SRTHSLPNDSY
|
1931-1941
|
13.49
|
nd
|
nd
|
nd
|
nd
|
Q19R08_HUMAN T calcium channel alpha 1G subunit variant 153 - Homo sapiens
|
Q19R10
|
APID
|
UniProt
|
SRTHSLPNDSY
|
1924-1934
|
13.49
|
nd
|
nd
|
nd
|
nd
|
Q19R10_HUMAN T calcium channel alpha 1G subunit variant 137 - Homo sapiens
|
Q19QY8
|
APID
|
UniProt
|
SRTHSLPNDSY
|
1952-1962
|
13.49
|
nd
|
nd
|
nd
|
nd
|
Q19QY8_HUMAN T calcium channel alpha 1G subunit variant 477 - Homo sapiens
|
Q19QZ0
|
APID
|
UniProt
|
SRTHSLPNDSY
|
1913-1923
|
13.49
|
nd
|
nd
|
nd
|
nd
|
Q19QZ0_HUMAN T calcium channel alpha 1G subunit variant 473-d75 - Homo sapiens
|
Q19QZ6
|
APID
|
UniProt
|
SRTHSLPNDSY
|
1956-1966
|
13.49
|
nd
|
nd
|
nd
|
nd
|
Q19QZ6_HUMAN T calcium channel alpha 1G subunit variant 249 - Homo sapiens
|
Q2TAC4
|
APID
|
UniProt
|
SRTHSLPNDSY
|
1926-1936
|
13.49
|
nd
|
nd
|
nd
|
nd
|
Q2TAC4_HUMAN Calcium channel, voltage-dependent, T type, alpha 1G subunit - Homo sapiens
|
Q19QZ1
|
APID
|
UniProt
|
SRTHSLPNDSY
|
1904-1914
|
13.49
|
nd
|
nd
|
nd
|
nd
|
Q19QZ1_HUMAN T calcium channel alpha 1G subunit variant 473 - Homo sapiens
|
Q19QZ2
|
APID
|
UniProt
|
SRTHSLPNDSY
|
1922-1932
|
13.49
|
nd
|
nd
|
nd
|
nd
|
Q19QZ2_HUMAN T calcium channel alpha 1G subunit variant 441-d81 - Homo sapiens
|
Q19R06
|
APID
|
UniProt
|
SRTHSLPNDSY
|
1942-1952
|
13.49
|
nd
|
nd
|
nd
|
nd
|
Q19R06_HUMAN T calcium channel alpha 1G subunit variant 169 - Homo sapiens
|
Q19R11
|
APID
|
UniProt
|
SRTHSLPNDSY
|
1963-1973
|
13.49
|
nd
|
nd
|
nd
|
nd
|
Q19R11_HUMAN T calcium channel alpha 1G subunit variant 93 - Homo sapiens
|
Q19QZ7
|
APID
|
UniProt
|
SRTHSLPNDSY
|
2031-2041
|
13.49
|
nd
|
nd
|
nd
|
nd
|
Q19QZ7_HUMAN T calcium channel alpha 1G subunit variant 223 - Homo sapiens
|
Q19QZ4
|
APID
|
UniProt
|
SRTHSLPNDSY
|
1897-1907
|
13.49
|
nd
|
nd
|
nd
|
nd
|
Q19QZ4_HUMAN T calcium channel alpha 1G subunit variant 409 - Homo sapiens
|
Q7Z5G3
|
APID
|
UniProt
|
PRRAASGPSGS
|
34-44
|
13.51
|
nd
|
nd
|
nd
|
nd
|
Q7Z5G3_HUMAN Acyl-CoA synthetase short-chain family member 1 - Homo sapiens
|