ENST00000317961.9:c.3274T>C
MANE Select
|
ENSP00000322408.4:p.Cys1092Arg
|
|
ENST00000317961.8:c.3274T>C
|
ENSP00000322408.4:p.Cys1092Arg
|
|
ENST00000382806.6:c.3103T>C
|
ENSP00000372256.2:p.Cys1035Arg
|
|
ENST00000415360.1:c.190T>C
|
ENSP00000389433.1:p.Cys64Arg
|
|
ENST00000440077.5:c.3151T>C
|
ENSP00000398543.1:p.Cys1051Arg
|
|
ENST00000469599.6:n.1872T>C
|
|
|
ENST00000492117.1:n.3166T>C
|
|
|
ENST00000541639.5:c.3367T>C
|
ENSP00000444293.1:p.Cys1123Arg
|
|
NM_001146705.1:c.3367T>C
|
NP_001140177.1:p.Cys1123Arg
|
|
NM_001146706.1:c.3103T>C
|
NP_001140178.1:p.Cys1035Arg
|
|
NM_004653.4:c.3274T>C
|
NP_004644.2:p.Cys1092Arg
|
|
XM_005262560.1:c.3139T>C
|
XP_005262617.1:p.Cys1047Arg
|
|
XM_005262561.1:c.3043T>C
|
XP_005262618.1:p.Cys1015Arg
|
|
XM_011531468.1:c.3196T>C
|
XP_011529770.1:p.Cys1066Arg
|
|
XR_244571.2:n.3562T>C
|
|
|
XR_430568.2:n.3896T>C
|
|
|
XM_005262560.3:c.3139T>C
|
XP_005262617.1:p.Cys1047Arg
|
|
XM_005262561.3:c.3043T>C
|
XP_005262618.1:p.Cys1015Arg
|
|
XM_011531468.3:c.3196T>C
|
XP_011529770.1:p.Cys1066Arg
|
|
XM_024452495.1:c.1264T>C
|
XP_024308263.1:p.Cys422Arg
|
|
XM_024452496.1:c.1030T>C
|
XP_024308264.1:p.Cys344Arg
|
|
XR_001756009.2:n.4012T>C
|
|
|
XR_001756010.2:n.4012T>C
|
|
|
XR_001756011.2:n.3877T>C
|
|
|
XR_001756012.2:n.4025T>C
|
|
|
XR_001756013.2:n.3343T>C
|
|
|
XR_002958832.1:n.3444T>C
|
|
|
XR_002958834.1:n.3668T>C
|
|
|
XR_002958835.1:n.3551T>C
|
|
|
XR_002958836.1:n.4234T>C
|
|
|
XR_002958837.1:n.4041T>C
|
|
|
XR_244571.4:n.3561T>C
|
|
|
XR_430568.4:n.3895T>C
|
|
|
NM_001146706.2:c.3103T>C
|
NP_001140178.1:p.Cys1035Arg
|
|
NM_004653.5:c.3274T>C
MANE Select
|
NP_004644.2:p.Cys1092Arg
|
|
NM_001146705.2:c.3367T>C
|
NP_001140177.1:p.Cys1123Arg
|
|