ENST00000695651.1:n.885A>T
|
|
|
ENST00000695652.1:c.2414A>T
|
ENSP00000512083.1:p.Glu805Val
|
|
ENST00000695653.1:c.446A>T
|
ENSP00000512084.1:p.Glu149Val
|
|
ENST00000695654.1:c.1661A>T
|
ENSP00000512085.1:p.Glu554Val
|
|
ENST00000695655.1:c.1478A>T
|
ENSP00000512086.1:n.1478A>T
|
|
ENST00000695692.1:n.1901A>T
|
|
|
ENST00000245907.11:c.2537A>T
MANE Select
|
ENSP00000245907.4:p.Glu846Val
|
|
ENST00000245907.10:c.2537A>T
|
ENSP00000245907.4:p.Glu846Val
|
|
ENST00000594005.1:n.18A>T
|
|
|
ENST00000602053.1:n.585A>T
|
|
|
NM_000064.3:c.2537A>T
|
NP_000055.2:p.Glu846Val
|
|
NM_000064.4:c.2537A>T
MANE Select
|
NP_000055.2:p.Glu846Val
|
|