|
Q6NXU0
|
APID
|
UniProt
|
GRRGRLPSKPKS
|
277-288
|
9.41
|
nd
|
nd
|
nd
|
nd
|
Q6NXU0_HUMAN Nuclear receptor subfamily 4, group A, member 2 - Homo sapiens
|
|
Q19R06
|
APID
|
UniProt
|
RLMLPPPSTPAL
|
531-542
|
9.41
|
nd
|
nd
|
nd
|
nd
|
Q19R06_HUMAN T calcium channel alpha 1G subunit variant 169 - Homo sapiens
|
|
Q19R10
|
APID
|
UniProt
|
RLMLPPPSTPAL
|
531-542
|
9.41
|
nd
|
nd
|
nd
|
nd
|
Q19R10_HUMAN T calcium channel alpha 1G subunit variant 137 - Homo sapiens
|
|
Q19QZ7
|
APID
|
UniProt
|
RLMLPPPSTPAL
|
531-542
|
9.41
|
nd
|
nd
|
nd
|
nd
|
Q19QZ7_HUMAN T calcium channel alpha 1G subunit variant 223 - Homo sapiens
|
|
Q19QZ6
|
APID
|
UniProt
|
RLMLPPPSTPAL
|
531-542
|
9.41
|
nd
|
nd
|
nd
|
nd
|
Q19QZ6_HUMAN T calcium channel alpha 1G subunit variant 249 - Homo sapiens
|
|
A8K9B8
|
APID
|
UniProt
|
FNEVRLPPPPDI
|
44-55
|
9.41
|
nd
|
nd
|
nd
|
nd
|
A8K9B8_HUMAN cDNA FLJ75450, highly similar to Homo sapiens fragile X mental retardation, autosomal homolog 1(FXR1), mRNA - Homo sapiens
|
|
A8K2I7
|
APID
|
UniProt
|
GPQMGLPPPPPA
|
42-53
|
9.41
|
nd
|
nd
|
nd
|
nd
|
A8K2I7_HUMAN cDNA FLJ76072, highly similar to Homo sapiens GIPC PDZ domain containing family, member 1 (GIPC1), transcript variant 1, mRNA - Homo sapiens
|
|
A2A3I7
|
APID
|
UniProt
|
GRRGRLPSKPKS
|
380-391
|
9.41
|
nd
|
nd
|
nd
|
nd
|
A2A3I7_HUMAN Nuclear receptor subfamily 4, group A, member 3 - Homo sapiens
|
|
Q19R09
|
APID
|
UniProt
|
RLMLPPPSTPAL
|
531-542
|
9.41
|
nd
|
nd
|
nd
|
nd
|
Q19R09_HUMAN T calcium channel alpha 1G subunit variant 145 - Homo sapiens
|
|
Q19QZ3
|
APID
|
UniProt
|
RLMLPPPSTPAL
|
531-542
|
9.41
|
nd
|
nd
|
nd
|
nd
|
Q19QZ3_HUMAN T calcium channel alpha 1G subunit variant 441 - Homo sapiens
|
|
Q19QZ8
|
APID
|
UniProt
|
RLMLPPPSTPAL
|
531-542
|
9.41
|
nd
|
nd
|
nd
|
nd
|
Q19QZ8_HUMAN T calcium channel alpha 1G subunit variant 221 - Homo sapiens
|
|
Q2TAC4
|
APID
|
UniProt
|
RLMLPPPSTPAL
|
531-542
|
9.41
|
nd
|
nd
|
nd
|
nd
|
Q2TAC4_HUMAN Calcium channel, voltage-dependent, T type, alpha 1G subunit - Homo sapiens
|
|
Q19R16
|
APID
|
UniProt
|
RLMLPPPSTPAL
|
531-542
|
9.41
|
nd
|
nd
|
nd
|
nd
|
Q19R16_HUMAN T calcium channel alpha 1G subunit variant 33 - Homo sapiens
|
|
Q9H6B5
|
APID
|
UniProt
|
PSVRSQPLERPL
|
716-727
|
9.41
|
nd
|
nd
|
nd
|
nd
|
Q9H6B5_HUMAN CDNA: FLJ22413 fis, clone HRC08475 - Homo sapiens
|
|
Q19R13
|
APID
|
UniProt
|
RLMLPPPSTPAL
|
531-542
|
9.41
|
nd
|
nd
|
nd
|
nd
|
Q19R13_HUMAN T calcium channel alpha 1G subunit variant 88 - Homo sapiens
|
|
Q19R17
|
APID
|
UniProt
|
RLMLPPPSTPAL
|
531-542
|
9.41
|
nd
|
nd
|
nd
|
nd
|
Q19R17_HUMAN T calcium channel alpha 1G subunit variant 25 - Homo sapiens
|
|
Q19R12
|
APID
|
UniProt
|
RLMLPPPSTPAL
|
531-542
|
9.41
|
nd
|
nd
|
nd
|
nd
|
Q19R12_HUMAN T calcium channel alpha 1G subunit variant 89 - Homo sapiens
|
|
Q19QY9
|
APID
|
UniProt
|
RLMLPPPSTPAL
|
531-542
|
9.41
|
nd
|
nd
|
nd
|
nd
|
Q19QY9_HUMAN T calcium channel alpha 1G subunit variant 473-d81 - Homo sapiens
|
|
O43497
|
APID
|
UniProt
|
RLMLPPPSTPAL
|
531-542
|
9.41
|
nd
|
nd
|
nd
|
nd
|
CAC1G_HUMAN Voltage-dependent T-type calcium channel subunit alpha-1G - Homo sapiens
|
|
Q19R15
|
APID
|
UniProt
|
RLMLPPPSTPAL
|
531-542
|
9.41
|
nd
|
nd
|
nd
|
nd
|
Q19R15_HUMAN T calcium channel alpha 1G subunit variant 49 - Homo sapiens
|