ENST00000695651.1:n.813A>T
|
|
|
ENST00000695652.1:c.2342A>T
|
ENSP00000512083.1:p.Glu781Val
|
|
ENST00000695653.1:c.374A>T
|
ENSP00000512084.1:p.Glu125Val
|
|
ENST00000695654.1:c.1589A>T
|
ENSP00000512085.1:p.Glu530Val
|
|
ENST00000695655.1:c.1406A>T
|
ENSP00000512086.1:n.1406A>T
|
|
ENST00000695692.1:n.1829A>T
|
|
|
ENST00000245907.11:c.2465A>T
MANE Select
|
ENSP00000245907.4:p.Glu822Val
|
|
ENST00000245907.10:c.2465A>T
|
ENSP00000245907.4:p.Glu822Val
|
|
ENST00000602053.1:n.513A>T
|
|
|
NM_000064.3:c.2465A>T
|
NP_000055.2:p.Glu822Val
|
|
NM_000064.4:c.2465A>T
MANE Select
|
NP_000055.2:p.Glu822Val
|
|