|
Q19QZ5
|
APID
|
UniProt
|
RQRSLGPD
|
712-719
|
8.68
|
nd
|
nd
|
nd
|
nd
|
Q19QZ5_HUMAN T calcium channel alpha 1G subunit variant 313 - Homo sapiens
|
|
Q19R08
|
APID
|
UniProt
|
RQRSLGPD
|
712-719
|
8.68
|
nd
|
nd
|
nd
|
nd
|
Q19R08_HUMAN T calcium channel alpha 1G subunit variant 153 - Homo sapiens
|
|
Q19QZ7
|
APID
|
UniProt
|
RQRSLGPD
|
712-719
|
8.68
|
nd
|
nd
|
nd
|
nd
|
Q19QZ7_HUMAN T calcium channel alpha 1G subunit variant 223 - Homo sapiens
|
|
Q19QY8
|
APID
|
UniProt
|
RQRSLGPD
|
712-719
|
8.68
|
nd
|
nd
|
nd
|
nd
|
Q19QY8_HUMAN T calcium channel alpha 1G subunit variant 477 - Homo sapiens
|
|
A8K4D8
|
APID
|
UniProt
|
NQRSSSFG
|
24-31
|
8.68
|
nd
|
nd
|
nd
|
nd
|
A8K4D8_HUMAN cDNA FLJ75325, highly similar to Homo sapiens sorting nexin 16 (SNX16), transcript variant 2, mRNA - Homo sapiens
|
|
Q8N9K7
|
APID
|
UniProt
|
RAESAGDR
|
28-35
|
8.68
|
nd
|
nd
|
nd
|
nd
|
CH079_HUMAN Uncharacterized protein C8orf79 - Homo sapiens
|
|
Q19R09
|
APID
|
UniProt
|
RQRSLGPD
|
712-719
|
8.68
|
nd
|
nd
|
nd
|
nd
|
Q19R09_HUMAN T calcium channel alpha 1G subunit variant 145 - Homo sapiens
|
|
Q19R18
|
APID
|
UniProt
|
RQRSLGPD
|
712-719
|
8.68
|
nd
|
nd
|
nd
|
nd
|
Q19R18_HUMAN T calcium channel alpha 1G subunit variant 17 - Homo sapiens
|
|
Q19R15
|
APID
|
UniProt
|
RQRSLGPD
|
712-719
|
8.68
|
nd
|
nd
|
nd
|
nd
|
Q19R15_HUMAN T calcium channel alpha 1G subunit variant 49 - Homo sapiens
|
|
Q19R10
|
APID
|
UniProt
|
RQRSLGPD
|
712-719
|
8.68
|
nd
|
nd
|
nd
|
nd
|
Q19R10_HUMAN T calcium channel alpha 1G subunit variant 137 - Homo sapiens
|
|
Q658L0
|
APID
|
UniProt
|
NQRSSSFG
|
24-31
|
8.68
|
nd
|
nd
|
nd
|
nd
|
Q658L0_HUMAN Putative uncharacterized protein DKFZp666H147 - Homo sapiens
|
|
Q9UPQ0
|
APID
|
UniProt
|
VLRGSSDG
|
221-228
|
8.68
|
nd
|
nd
|
nd
|
nd
|
LIMC1_HUMAN LIM and calponin homology domains-containing protein 1 - Homo sapiens
|
|
Q19QZ6
|
APID
|
UniProt
|
RQRSLGPD
|
712-719
|
8.68
|
nd
|
nd
|
nd
|
nd
|
Q19QZ6_HUMAN T calcium channel alpha 1G subunit variant 249 - Homo sapiens
|
|
O43497
|
APID
|
UniProt
|
RQRSLGPD
|
712-719
|
8.68
|
nd
|
nd
|
nd
|
nd
|
CAC1G_HUMAN Voltage-dependent T-type calcium channel subunit alpha-1G - Homo sapiens
|
|
Q19R05
|
APID
|
UniProt
|
RQRSLGPD
|
712-719
|
8.68
|
nd
|
nd
|
nd
|
nd
|
Q19R05_HUMAN T calcium channel alpha 1G subunit variant 177 - Homo sapiens
|
|
Q5JYA6
|
APID
|
UniProt
|
RVDSNGAP
|
92-99
|
8.68
|
nd
|
nd
|
nd
|
nd
|
Q5JYA6_HUMAN Pleckstrin homology domain containing, family G (With RhoGef domain) member 1 - Homo sapiens
|
|
Q19QZ8
|
APID
|
UniProt
|
RQRSLGPD
|
712-719
|
8.68
|
nd
|
nd
|
nd
|
nd
|
Q19QZ8_HUMAN T calcium channel alpha 1G subunit variant 221 - Homo sapiens
|
|
Q19QZ0
|
APID
|
UniProt
|
RQRSLGPD
|
712-719
|
8.68
|
nd
|
nd
|
nd
|
nd
|
Q19QZ0_HUMAN T calcium channel alpha 1G subunit variant 473-d75 - Homo sapiens
|
|
Q19R04
|
APID
|
UniProt
|
RQRSLGPD
|
712-719
|
8.68
|
nd
|
nd
|
nd
|
nd
|
Q19R04_HUMAN T calcium channel alpha 1G subunit variant 184 - Homo sapiens
|
|
Q19R03
|
APID
|
UniProt
|
RQRSLGPD
|
712-719
|
8.68
|
nd
|
nd
|
nd
|
nd
|
Q19R03_HUMAN T calcium channel alpha 1G subunit variant 185 - Homo sapiens
|