ENST00000695651.1:n.1081A>G
|
|
|
ENST00000695652.1:c.2610A>G
|
ENSP00000512083.1:p.Glu870=
|
|
ENST00000695653.1:c.642A>G
|
ENSP00000512084.1:p.Glu214=
|
|
ENST00000695654.1:c.1857A>G
|
ENSP00000512085.1:p.Glu619=
|
|
ENST00000695655.1:c.1674A>G
|
ENSP00000512086.1:n.1674A>G
|
|
ENST00000695692.1:n.2097A>G
|
|
|
ENST00000245907.11:c.2733A>G
MANE Select
|
ENSP00000245907.4:p.Glu911=
|
|
ENST00000245907.10:c.2733A>G
|
ENSP00000245907.4:p.Glu911=
|
|
ENST00000594005.1:n.309A>G
|
|
|
NM_000064.3:c.2733A>G
|
NP_000055.2:p.Glu911=
|
|
NM_000064.4:c.2733A>G
MANE Select
|
NP_000055.2:p.Glu911=
|
|