ENST00000695651.1:n.925G>T
|
|
|
ENST00000695652.1:c.2454G>T
|
ENSP00000512083.1:p.Glu818Asp
|
|
ENST00000695653.1:c.486G>T
|
ENSP00000512084.1:p.Glu162Asp
|
|
ENST00000695654.1:c.1701G>T
|
ENSP00000512085.1:p.Glu567Asp
|
|
ENST00000695655.1:c.1518G>T
|
ENSP00000512086.1:n.1518G>T
|
|
ENST00000695692.1:n.1941G>T
|
|
|
ENST00000245907.11:c.2577G>T
MANE Select
|
ENSP00000245907.4:p.Glu859Asp
|
|
ENST00000245907.10:c.2577G>T
|
ENSP00000245907.4:p.Glu859Asp
|
|
ENST00000594005.1:n.58G>T
|
|
|
NM_000064.3:c.2577G>T
|
NP_000055.2:p.Glu859Asp
|
|
NM_000064.4:c.2577G>T
MANE Select
|
NP_000055.2:p.Glu859Asp
|
|