ENST00000317961.9:c.3576T>C
MANE Select
|
ENSP00000322408.4:p.Cys1192=
|
|
ENST00000317961.8:c.3576T>C
|
ENSP00000322408.4:p.Cys1192=
|
|
ENST00000382806.6:c.3405T>C
|
ENSP00000372256.2:p.Cys1135=
|
|
ENST00000415360.1:c.492T>C
|
ENSP00000389433.1:p.Cys164=
|
|
ENST00000440077.5:c.3453T>C
|
ENSP00000398543.1:p.Cys1151=
|
|
ENST00000469599.6:n.2174T>C
|
|
|
ENST00000492117.1:n.3468T>C
|
|
|
ENST00000541639.5:c.3669T>C
|
ENSP00000444293.1:p.Cys1223=
|
|
NM_001146705.1:c.3669T>C
|
NP_001140177.1:p.Cys1223=
|
|
NM_001146706.1:c.3405T>C
|
NP_001140178.1:p.Cys1135=
|
|
NM_004653.4:c.3576T>C
|
NP_004644.2:p.Cys1192=
|
|
XM_005262560.1:c.3441T>C
|
XP_005262617.1:p.Cys1147=
|
|
XM_005262561.1:c.3345T>C
|
XP_005262618.1:p.Cys1115=
|
|
XM_011531468.1:c.3498T>C
|
XP_011529770.1:p.Cys1166=
|
|
XR_244571.2:n.3864T>C
|
|
|
XR_430568.2:n.4198T>C
|
|
|
XM_005262560.3:c.3441T>C
|
XP_005262617.1:p.Cys1147=
|
|
XM_005262561.3:c.3345T>C
|
XP_005262618.1:p.Cys1115=
|
|
XM_011531468.3:c.3498T>C
|
XP_011529770.1:p.Cys1166=
|
|
XM_024452495.1:c.1566T>C
|
XP_024308263.1:p.Cys522=
|
|
XM_024452496.1:c.1332T>C
|
XP_024308264.1:p.Cys444=
|
|
XR_001756009.2:n.4314T>C
|
|
|
XR_001756010.2:n.4314T>C
|
|
|
XR_001756011.2:n.4179T>C
|
|
|
XR_001756012.2:n.4327T>C
|
|
|
XR_001756013.2:n.3645T>C
|
|
|
XR_002958832.1:n.3746T>C
|
|
|
XR_002958834.1:n.3970T>C
|
|
|
XR_002958835.1:n.3853T>C
|
|
|
XR_002958836.1:n.4536T>C
|
|
|
XR_002958837.1:n.4343T>C
|
|
|
XR_244571.4:n.3863T>C
|
|
|
XR_430568.4:n.4197T>C
|
|
|
NM_001146706.2:c.3405T>C
|
NP_001140178.1:p.Cys1135=
|
|
NM_004653.5:c.3576T>C
MANE Select
|
NP_004644.2:p.Cys1192=
|
|
NM_001146705.2:c.3669T>C
|
NP_001140177.1:p.Cys1223=
|
|