ENST00000695651.1:n.1080A>T
|
|
|
ENST00000695652.1:c.2609A>T
|
ENSP00000512083.1:p.Glu870Val
|
|
ENST00000695653.1:c.641A>T
|
ENSP00000512084.1:p.Glu214Val
|
|
ENST00000695654.1:c.1856A>T
|
ENSP00000512085.1:p.Glu619Val
|
|
ENST00000695655.1:c.1673A>T
|
ENSP00000512086.1:n.1673A>T
|
|
ENST00000695692.1:n.2096A>T
|
|
|
ENST00000245907.11:c.2732A>T
MANE Select
|
ENSP00000245907.4:p.Glu911Val
|
|
ENST00000245907.10:c.2732A>T
|
ENSP00000245907.4:p.Glu911Val
|
|
ENST00000594005.1:n.308A>T
|
|
|
NM_000064.3:c.2732A>T
|
NP_000055.2:p.Glu911Val
|
|
NM_000064.4:c.2732A>T
MANE Select
|
NP_000055.2:p.Glu911Val
|
|