ENST00000695651.1:n.943A>G
|
|
|
ENST00000695652.1:c.2472A>G
|
ENSP00000512083.1:p.Glu824=
|
|
ENST00000695653.1:c.504A>G
|
ENSP00000512084.1:p.Glu168=
|
|
ENST00000695654.1:c.1719A>G
|
ENSP00000512085.1:p.Glu573=
|
|
ENST00000695655.1:c.1536A>G
|
ENSP00000512086.1:n.1536A>G
|
|
ENST00000695692.1:n.1959A>G
|
|
|
ENST00000245907.11:c.2595A>G
MANE Select
|
ENSP00000245907.4:p.Glu865=
|
|
ENST00000245907.10:c.2595A>G
|
ENSP00000245907.4:p.Glu865=
|
|
ENST00000594005.1:n.171A>G
|
|
|
NM_000064.3:c.2595A>G
|
NP_000055.2:p.Glu865=
|
|
NM_000064.4:c.2595A>G
MANE Select
|
NP_000055.2:p.Glu865=
|
|