ENST00000695651.1:n.1074A>T
|
|
|
ENST00000695652.1:c.2603A>T
|
ENSP00000512083.1:p.Glu868Val
|
|
ENST00000695653.1:c.635A>T
|
ENSP00000512084.1:p.Glu212Val
|
|
ENST00000695654.1:c.1850A>T
|
ENSP00000512085.1:p.Glu617Val
|
|
ENST00000695655.1:c.1667A>T
|
ENSP00000512086.1:n.1667A>T
|
|
ENST00000695692.1:n.2090A>T
|
|
|
ENST00000245907.11:c.2726A>T
MANE Select
|
ENSP00000245907.4:p.Glu909Val
|
|
ENST00000245907.10:c.2726A>T
|
ENSP00000245907.4:p.Glu909Val
|
|
ENST00000594005.1:n.302A>T
|
|
|
NM_000064.3:c.2726A>T
|
NP_000055.2:p.Glu909Val
|
|
NM_000064.4:c.2726A>T
MANE Select
|
NP_000055.2:p.Glu909Val
|
|