ENST00000317961.9:c.3567T>A
MANE Select
|
ENSP00000322408.4:p.Cys1189Ter
|
|
ENST00000317961.8:c.3567T>A
|
ENSP00000322408.4:p.Cys1189Ter
|
|
ENST00000382806.6:c.3396T>A
|
ENSP00000372256.2:p.Cys1132Ter
|
|
ENST00000415360.1:c.483T>A
|
ENSP00000389433.1:p.Cys161Ter
|
|
ENST00000440077.5:c.3444T>A
|
ENSP00000398543.1:p.Cys1148Ter
|
|
ENST00000469599.6:n.2165T>A
|
|
|
ENST00000492117.1:n.3459T>A
|
|
|
ENST00000541639.5:c.3660T>A
|
ENSP00000444293.1:p.Cys1220Ter
|
|
NM_001146705.1:c.3660T>A
|
NP_001140177.1:p.Cys1220Ter
|
|
NM_001146706.1:c.3396T>A
|
NP_001140178.1:p.Cys1132Ter
|
|
NM_004653.4:c.3567T>A
|
NP_004644.2:p.Cys1189Ter
|
|
XM_005262560.1:c.3432T>A
|
XP_005262617.1:p.Cys1144Ter
|
|
XM_005262561.1:c.3336T>A
|
XP_005262618.1:p.Cys1112Ter
|
|
XM_011531468.1:c.3489T>A
|
XP_011529770.1:p.Cys1163Ter
|
|
XR_244571.2:n.3855T>A
|
|
|
XR_430568.2:n.4189T>A
|
|
|
XM_005262560.3:c.3432T>A
|
XP_005262617.1:p.Cys1144Ter
|
|
XM_005262561.3:c.3336T>A
|
XP_005262618.1:p.Cys1112Ter
|
|
XM_011531468.3:c.3489T>A
|
XP_011529770.1:p.Cys1163Ter
|
|
XM_024452495.1:c.1557T>A
|
XP_024308263.1:p.Cys519Ter
|
|
XM_024452496.1:c.1323T>A
|
XP_024308264.1:p.Cys441Ter
|
|
XR_001756009.2:n.4305T>A
|
|
|
XR_001756010.2:n.4305T>A
|
|
|
XR_001756011.2:n.4170T>A
|
|
|
XR_001756012.2:n.4318T>A
|
|
|
XR_001756013.2:n.3636T>A
|
|
|
XR_002958832.1:n.3737T>A
|
|
|
XR_002958834.1:n.3961T>A
|
|
|
XR_002958835.1:n.3844T>A
|
|
|
XR_002958836.1:n.4527T>A
|
|
|
XR_002958837.1:n.4334T>A
|
|
|
XR_244571.4:n.3854T>A
|
|
|
XR_430568.4:n.4188T>A
|
|
|
NM_001146706.2:c.3396T>A
|
NP_001140178.1:p.Cys1132Ter
|
|
NM_004653.5:c.3567T>A
MANE Select
|
NP_004644.2:p.Cys1189Ter
|
|
NM_001146705.2:c.3660T>A
|
NP_001140177.1:p.Cys1220Ter
|
|