ENST00000695651.1:n.892A>G
|
|
|
ENST00000695652.1:c.2421A>G
|
ENSP00000512083.1:p.Arg807=
|
|
ENST00000695653.1:c.453A>G
|
ENSP00000512084.1:p.Arg151=
|
|
ENST00000695654.1:c.1668A>G
|
ENSP00000512085.1:p.Arg556=
|
|
ENST00000695655.1:c.1485A>G
|
ENSP00000512086.1:n.1485A>G
|
|
ENST00000695692.1:n.1908A>G
|
|
|
ENST00000245907.11:c.2544A>G
MANE Select
|
ENSP00000245907.4:p.Arg848=
|
|
ENST00000245907.10:c.2544A>G
|
ENSP00000245907.4:p.Arg848=
|
|
ENST00000594005.1:n.25A>G
|
|
|
ENST00000602053.1:n.592A>G
|
|
|
NM_000064.3:c.2544A>G
|
NP_000055.2:p.Arg848=
|
|
NM_000064.4:c.2544A>G
MANE Select
|
NP_000055.2:p.Arg848=
|
|