ENST00000675795.1:c.2261A>T
MANE Select
|
ENSP00000501699.1:p.Asp754Val
|
|
ENST00000286301.7:c.2261A>T
|
ENSP00000286301.3:p.Asp754Val
|
|
ENST00000504875.5:c.*82A>T
|
ENSP00000422212.1:n.*82A>T
|
|
ENST00000515068.1:c.430A>T
|
ENSP00000427545.1:n.430A>T
|
|
NM_001288705.1:c.2261A>T
|
NP_001275634.1:p.Asp754Val
|
|
NM_005211.3:c.2261A>T
|
NP_005202.2:p.Asp754Val
|
|
NR_109969.1:n.2311A>T
|
|
|
NM_001288705.2:c.2261A>T
|
NP_001275634.1:p.Asp754Val
|
|
NM_001349736.1:c.2261A>T
|
NP_001336665.1:p.Asp754Val
|
|
NM_001288705.3:c.2261A>T
MANE Select
|
NP_001275634.1:p.Asp754Val
|
|
NM_001375320.1:c.2261A>T
|
NP_001362249.1:p.Asp754Val
|
|
NM_001375321.1:c.1817A>T
|
NP_001362250.1:p.Asp606Val
|
|
NR_164679.1:n.2154A>T
|
|
|
NM_001349736.2:c.2261A>T
|
NP_001336665.1:p.Asp754Val
|
|
NM_005211.4:c.2261A>T
|
NP_005202.2:p.Asp754Val
|
|
NR_109969.2:n.2225A>T
|
|
|