ENST00000317961.9:c.3574T>C
MANE Select
|
ENSP00000322408.4:p.Cys1192Arg
|
|
ENST00000317961.8:c.3574T>C
|
ENSP00000322408.4:p.Cys1192Arg
|
|
ENST00000382806.6:c.3403T>C
|
ENSP00000372256.2:p.Cys1135Arg
|
|
ENST00000415360.1:c.490T>C
|
ENSP00000389433.1:p.Cys164Arg
|
|
ENST00000440077.5:c.3451T>C
|
ENSP00000398543.1:p.Cys1151Arg
|
|
ENST00000469599.6:n.2172T>C
|
|
|
ENST00000492117.1:n.3466T>C
|
|
|
ENST00000541639.5:c.3667T>C
|
ENSP00000444293.1:p.Cys1223Arg
|
|
NM_001146705.1:c.3667T>C
|
NP_001140177.1:p.Cys1223Arg
|
|
NM_001146706.1:c.3403T>C
|
NP_001140178.1:p.Cys1135Arg
|
|
NM_004653.4:c.3574T>C
|
NP_004644.2:p.Cys1192Arg
|
|
XM_005262560.1:c.3439T>C
|
XP_005262617.1:p.Cys1147Arg
|
|
XM_005262561.1:c.3343T>C
|
XP_005262618.1:p.Cys1115Arg
|
|
XM_011531468.1:c.3496T>C
|
XP_011529770.1:p.Cys1166Arg
|
|
XR_244571.2:n.3862T>C
|
|
|
XR_430568.2:n.4196T>C
|
|
|
XM_005262560.3:c.3439T>C
|
XP_005262617.1:p.Cys1147Arg
|
|
XM_005262561.3:c.3343T>C
|
XP_005262618.1:p.Cys1115Arg
|
|
XM_011531468.3:c.3496T>C
|
XP_011529770.1:p.Cys1166Arg
|
|
XM_024452495.1:c.1564T>C
|
XP_024308263.1:p.Cys522Arg
|
|
XM_024452496.1:c.1330T>C
|
XP_024308264.1:p.Cys444Arg
|
|
XR_001756009.2:n.4312T>C
|
|
|
XR_001756010.2:n.4312T>C
|
|
|
XR_001756011.2:n.4177T>C
|
|
|
XR_001756012.2:n.4325T>C
|
|
|
XR_001756013.2:n.3643T>C
|
|
|
XR_002958832.1:n.3744T>C
|
|
|
XR_002958834.1:n.3968T>C
|
|
|
XR_002958835.1:n.3851T>C
|
|
|
XR_002958836.1:n.4534T>C
|
|
|
XR_002958837.1:n.4341T>C
|
|
|
XR_244571.4:n.3861T>C
|
|
|
XR_430568.4:n.4195T>C
|
|
|
NM_001146706.2:c.3403T>C
|
NP_001140178.1:p.Cys1135Arg
|
|
NM_004653.5:c.3574T>C
MANE Select
|
NP_004644.2:p.Cys1192Arg
|
|
NM_001146705.2:c.3667T>C
|
NP_001140177.1:p.Cys1223Arg
|
|