ENST00000700029.2:c.1243G>T
|
ENSP00000514759.2:p.Asp415Tyr
|
|
ENST00000710265.1:c.*179G>T
|
ENSP00000518161.1:n.*179G>T
|
|
ENST00000688158.2:n.1885G>T
|
|
|
ENST00000688922.2:c.*980G>T
|
ENSP00000508742.2:n.*980G>T
|
|
ENST00000700021.1:c.1105G>T
|
ENSP00000514757.1:p.Asp369Tyr
|
|
ENST00000700022.1:c.*489G>T
|
ENSP00000514758.1:n.*489G>T
|
|
ENST00000700023.1:n.2308G>T
|
|
|
ENST00000700024.1:n.2542G>T
|
|
|
ENST00000706954.1:c.1150G>T
|
ENSP00000516674.1:p.Asp384Tyr
|
|
ENST00000706955.1:c.*1185G>T
|
ENSP00000516675.1:n.*1185G>T
|
|
ENST00000686459.1:c.*736G>T
|
ENSP00000508909.1:n.*736G>T
|
|
ENST00000688158.1:c.*1261G>T
|
ENSP00000509254.1:n.*1261G>T
|
|
ENST00000688308.1:c.1150G>T
|
ENSP00000508752.1:p.Asp384Tyr
|
|
ENST00000688922.1:c.1071G>T
|
|
|
ENST00000693560.1:c.1669G>T
|
ENSP00000509861.1:p.Asp557Tyr
|
|
ENST00000371953.8:c.1150G>T
MANE Select
|
ENSP00000361021.3:p.Asp384Tyr
|
|
ENST00000371953.7:c.1150G>T
|
ENSP00000361021.3:p.Asp384Tyr
|
|
NM_000314.5:c.1150G>T
|
NP_000305.3:p.Asp384Tyr
|
|
NM_000314.6:c.1150G>T
|
NP_000305.3:p.Asp384Tyr
|
|
NM_001304717.2:c.1669G>T
|
NP_001291646.2:p.Asp557Tyr
|
|
NM_001304718.1:c.559G>T
|
NP_001291647.1:p.Asp187Tyr
|
|
XM_006717926.2:c.1105G>T
|
XP_006717989.1:p.Asp369Tyr
|
|
XM_011539982.1:c.1054G>T
|
XP_011538284.1:p.Asp352Tyr
|
|
XR_945791.1:n.1720G>T
|
|
|
NM_000314.7:c.1150G>T
|
NP_000305.3:p.Asp384Tyr
|
|
NM_001304717.5:c.1669G>T
|
NP_001291646.4:p.Asp557Tyr
|
|
NM_001304718.2:c.559G>T
|
NP_001291647.1:p.Asp187Tyr
|
|
NM_000314.8:c.1150G>T
MANE Select
|
NP_000305.3:p.Asp384Tyr
|
|