|
Q19QZ4
|
APID
|
UniProt
|
PKLPPPGRSP
|
1970-1979
|
4.1
|
nd
|
nd
|
nd
|
nd
|
Q19QZ4_HUMAN T calcium channel alpha 1G subunit variant 409 - Homo sapiens
|
|
P41225
|
APID
|
UniProt
|
PPPALPPMHR
|
292-301
|
4.1
|
nd
|
nd
|
nd
|
nd
|
SOX3_HUMAN Transcription factor SOX-3 - Homo sapiens
|
|
Q2XND2
|
APID
|
UniProt
|
GPLPLPGLGN
|
36-45
|
4.1
|
nd
|
nd
|
nd
|
nd
|
Q2XND2_HUMAN Cytochrome P450 2D6 - Homo sapiens
|
|
Q19QY9
|
APID
|
UniProt
|
PKLPPPGRSP
|
1984-1993
|
4.1
|
nd
|
nd
|
nd
|
nd
|
Q19QY9_HUMAN T calcium channel alpha 1G subunit variant 473-d81 - Homo sapiens
|
|
P10635
|
APID
|
UniProt
|
GPLPLPGLGN
|
36-45
|
4.1
|
nd
|
nd
|
nd
|
nd
|
CP2D6_HUMAN Cytochrome P450 2D6 - Homo sapiens
|
|
Q2XNE0
|
APID
|
UniProt
|
GPLPLPGLGN
|
36-45
|
4.1
|
nd
|
nd
|
nd
|
nd
|
Q2XNE0_HUMAN Cytochrome P450 2D6 - Homo sapiens
|
|
Q16753
|
APID
|
UniProt
|
GPLPLPGLGN
|
36-45
|
4.1
|
nd
|
nd
|
nd
|
nd
|
Q16753_HUMAN Debrisoquine 4-hydroxylase mutant allele - Homo sapiens
|
|
Q16584
|
APID
|
UniProt
|
SPQPAPRRAP
|
793-802
|
4.1
|
nd
|
nd
|
nd
|
nd
|
M3K11_HUMAN Mitogen-activated protein kinase kinase kinase 11 - Homo sapiens
|
|
Q19QY8
|
APID
|
UniProt
|
PKLPPPGRSP
|
2025-2034
|
4.1
|
nd
|
nd
|
nd
|
nd
|
Q19QY8_HUMAN T calcium channel alpha 1G subunit variant 477 - Homo sapiens
|
|
A9QKR9
|
APID
|
UniProt
|
GPLPLPGLGN
|
36-45
|
4.1
|
nd
|
nd
|
nd
|
nd
|
A9QKR9_HUMAN Nonfunctional cytochrome P450 2D6 variant - Homo sapiens
|
|
Q19R03
|
APID
|
UniProt
|
PKLPPPGRSP
|
2022-2031
|
4.1
|
nd
|
nd
|
nd
|
nd
|
Q19R03_HUMAN T calcium channel alpha 1G subunit variant 185 - Homo sapiens
|
|
Q19QZ8
|
APID
|
UniProt
|
PKLPPPGRSP
|
2059-2068
|
4.1
|
nd
|
nd
|
nd
|
nd
|
Q19QZ8_HUMAN T calcium channel alpha 1G subunit variant 221 - Homo sapiens
|
|
A4D0Y1
|
APID
|
UniProt
|
GPPPPPARGR
|
278-287
|
4.1
|
nd
|
nd
|
nd
|
nd
|
A4D0Y1_HUMAN Wiskott-Aldrich syndrome-like - Homo sapiens
|
|
Q38LG2
|
APID
|
UniProt
|
GPLPLPGLGN
|
36-45
|
4.1
|
nd
|
nd
|
nd
|
nd
|
Q38LG2_HUMAN Cytochrome P450 2D6 - Homo sapiens
|
|
Q8NEZ4
|
APID
|
UniProt
|
PFIAPPGRVL
|
2956-2965
|
4.1
|
nd
|
nd
|
nd
|
nd
|
MLL3_HUMAN Myeloid/lymphoid or mixed-lineage leukemia protein 3 homolog - Homo sapiens
|
|
Q19R10
|
APID
|
UniProt
|
PKLPPPGRSP
|
1997-2006
|
4.1
|
nd
|
nd
|
nd
|
nd
|
Q19R10_HUMAN T calcium channel alpha 1G subunit variant 137 - Homo sapiens
|
|
O75342
|
APID
|
UniProt
|
SYVHIPSYRP
|
155-164
|
4.1
|
nd
|
nd
|
nd
|
nd
|
LX12B_HUMAN Arachidonate 12-lipoxygenase, 12R type - Homo sapiens
|
|
Q58A55
|
APID
|
UniProt
|
LSPDRPIRDT
|
99-108
|
4.1
|
nd
|
nd
|
nd
|
nd
|
Q58A55_HUMAN UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 11 - Homo sapiens
|
|
O00401
|
APID
|
UniProt
|
GPPPPPARGR
|
298-307
|
4.1
|
nd
|
nd
|
nd
|
nd
|
WASL_HUMAN Neural Wiskott-Aldrich syndrome protein - Homo sapiens
|
|
Q3KPF3
|
APID
|
UniProt
|
GPLPLPGLGN
|
36-45
|
4.1
|
nd
|
nd
|
nd
|
nd
|
Q3KPF3_HUMAN Cytochrome P450, family 2, subfamily D, polypeptide 6 - Homo sapiens
|