ENST00000209873.9:c.1428A>G
MANE Select
|
ENSP00000209873.4:p.Thr476=
|
|
ENST00000546562.6:n.2492A>G
|
|
|
ENST00000547238.6:n.2064A>G
|
|
|
ENST00000547520.6:n.1544A>G
|
|
|
ENST00000547757.2:c.*346A>G
|
ENSP00000448020.2:n.*346A>G
|
|
ENST00000548880.2:n.1878A>G
|
|
|
ENST00000548931.6:c.863A>G
|
ENSP00000457518.1:p.Gln288Arg
|
|
ENST00000549450.6:n.1362A>G
|
|
|
ENST00000552161.6:n.2506A>G
|
|
|
ENST00000672797.1:n.1917A>G
|
|
|
ENST00000209873.8:c.1428A>G
|
ENSP00000209873.4:p.Thr476=
|
|
ENST00000394384.7:c.1329A>G
|
ENSP00000377908.3:p.Thr443=
|
|
ENST00000548931.5:c.863A>G
|
ENSP00000457518.1:p.Gln288Arg
|
|
ENST00000550286.5:c.1056A>G
|
ENSP00000446885.1:p.Thr352=
|
|
ENST00000552876.5:n.1771A>G
|
|
|
NM_001173466.1:c.1329A>G
|
NP_001166937.1:p.Thr443=
|
|
NM_015665.5:c.1428A>G
|
NP_056480.1:p.Thr476=
|
|
XM_006719617.2:c.1443A>G
|
XP_006719680.1:p.Thr481=
|
|
XM_011538777.1:c.1485A>G
|
XP_011537079.1:p.Thr495=
|
|
XM_011538778.1:c.1470A>G
|
XP_011537080.1:p.Thr490=
|
|
XM_011538779.1:c.1386A>G
|
XP_011537081.1:p.Thr462=
|
|
XM_011538780.1:c.1371A>G
|
XP_011537082.1:p.Thr457=
|
|
XM_011538781.1:c.819A>G
|
XP_011537083.1:p.Thr273=
|
|
XM_011538778.2:c.1470A>G
|
XP_011537080.1:p.Thr490=
|
|
XM_011538780.2:c.1371A>G
|
XP_011537082.1:p.Thr457=
|
|
XR_001748875.2:n.1485A>G
|
|
|
NM_015665.6:c.1428A>G
MANE Select
|
NP_056480.1:p.Thr476=
|
|
NM_001173466.2:c.1329A>G
|
NP_001166937.1:p.Thr443=
|
|