|
Q19QZ1
|
APID
|
UniProt
|
SRTHSLPNDSYMCR
|
1904-1917
|
30.5
|
nd
|
nd
|
nd
|
nd
|
Q19QZ1_HUMAN T calcium channel alpha 1G subunit variant 473 - Homo sapiens
|
|
A8K5X0
|
APID
|
UniProt
|
GCGHRLSSTGHSMT
|
162-175
|
30.5
|
nd
|
nd
|
nd
|
nd
|
A8K5X0_HUMAN cDNA FLJ76311, highly similar to Homo sapiens kelch-like 1 (KLHL1), mRNA - Homo sapiens
|
|
Q19R17
|
APID
|
UniProt
|
SRTHSLPNDSYMCR
|
1908-1921
|
30.5
|
nd
|
nd
|
nd
|
nd
|
Q19R17_HUMAN T calcium channel alpha 1G subunit variant 25 - Homo sapiens
|
|
Q19QY8
|
APID
|
UniProt
|
SRTHSLPNDSYMCR
|
1952-1965
|
30.5
|
nd
|
nd
|
nd
|
nd
|
Q19QY8_HUMAN T calcium channel alpha 1G subunit variant 477 - Homo sapiens
|
|
Q19R02
|
APID
|
UniProt
|
SRTHSLPNDSYMCR
|
1997-2010
|
30.5
|
nd
|
nd
|
nd
|
nd
|
Q19R02_HUMAN T calcium channel alpha 1G subunit variant 189 - Homo sapiens
|
|
Q19R00
|
APID
|
UniProt
|
SRTHSLPNDSYMCR
|
1938-1951
|
30.5
|
nd
|
nd
|
nd
|
nd
|
Q19R00_HUMAN T calcium channel alpha 1G subunit variant 216 - Homo sapiens
|
|
A7E2A6
|
APID
|
UniProt
|
QDRRWTNPDGTTSK
|
1351-1364
|
30.5
|
nd
|
nd
|
nd
|
nd
|
A7E2A6_HUMAN Tensin like C1 domain containing phosphatase - Homo sapiens
|
|
Q19QZ8
|
APID
|
UniProt
|
SRTHSLPNDSYMCR
|
1986-1999
|
30.5
|
nd
|
nd
|
nd
|
nd
|
Q19QZ8_HUMAN T calcium channel alpha 1G subunit variant 221 - Homo sapiens
|
|
Q19R10
|
APID
|
UniProt
|
SRTHSLPNDSYMCR
|
1924-1937
|
30.5
|
nd
|
nd
|
nd
|
nd
|
Q19R10_HUMAN T calcium channel alpha 1G subunit variant 137 - Homo sapiens
|
|
O43497
|
APID
|
UniProt
|
SRTHSLPNDSYMCR
|
2042-2055
|
30.5
|
nd
|
nd
|
nd
|
nd
|
CAC1G_HUMAN Voltage-dependent T-type calcium channel subunit alpha-1G - Homo sapiens
|
|
Q7Z3C6
|
APID
|
UniProt
|
RSASYPCAAPRPGA
|
758-771
|
30.5
|
nd
|
nd
|
nd
|
nd
|
ATG9A_HUMAN Autophagy-related protein 9A - Homo sapiens
|
|
Q19R13
|
APID
|
UniProt
|
SRTHSLPNDSYMCR
|
1915-1928
|
30.5
|
nd
|
nd
|
nd
|
nd
|
Q19R13_HUMAN T calcium channel alpha 1G subunit variant 88 - Homo sapiens
|
|
Q19R07
|
APID
|
UniProt
|
SRTHSLPNDSYMCR
|
1979-1992
|
30.5
|
nd
|
nd
|
nd
|
nd
|
Q19R07_HUMAN T calcium channel alpha 1G subunit variant 157 - Homo sapiens
|
|
A3KMQ0
|
APID
|
UniProt
|
PLPLTKPRSISFPS
|
514-527
|
30.5
|
nd
|
nd
|
nd
|
nd
|
A3KMQ0_HUMAN FYVE, RhoGEF and PH domain containing 5 - Homo sapiens
|
|
Q19QZ6
|
APID
|
UniProt
|
SRTHSLPNDSYMCR
|
1956-1969
|
30.5
|
nd
|
nd
|
nd
|
nd
|
Q19QZ6_HUMAN T calcium channel alpha 1G subunit variant 249 - Homo sapiens
|
|
Q19QZ7
|
APID
|
UniProt
|
SRTHSLPNDSYMCR
|
2031-2044
|
30.5
|
nd
|
nd
|
nd
|
nd
|
Q19QZ7_HUMAN T calcium channel alpha 1G subunit variant 223 - Homo sapiens
|
|
Q8NEY1
|
APID
|
UniProt
|
GIARPSTSGSFGYK
|
595-608
|
30.5
|
nd
|
nd
|
nd
|
nd
|
NAV1_HUMAN Neuron navigator 1 - Homo sapiens
|
|
Q19QZ5
|
APID
|
UniProt
|
SRTHSLPNDSYMCR
|
1892-1905
|
30.5
|
nd
|
nd
|
nd
|
nd
|
Q19QZ5_HUMAN T calcium channel alpha 1G subunit variant 313 - Homo sapiens
|
|
A8K140
|
APID
|
UniProt
|
RSASYPCAAPRPGA
|
758-771
|
30.5
|
nd
|
nd
|
nd
|
nd
|
A8K140_HUMAN cDNA FLJ77748 - Homo sapiens
|
|
A8MYP5
|
APID
|
UniProt
|
RISSRGPGPHAHKA
|
12-25
|
30.5
|
nd
|
nd
|
nd
|
nd
|
A8MYP5_HUMAN Uncharacterized protein ENSP00000381738 - Homo sapiens
|