ENST00000695651.1:n.2083C>G
|
|
|
ENST00000695652.1:c.3612C>G
|
ENSP00000512083.1:p.Asp1204Glu
|
|
ENST00000695653.1:c.1644C>G
|
ENSP00000512084.1:p.Asp548Glu
|
|
ENST00000695654.1:c.2760C>G
|
ENSP00000512085.1:p.Asp920Glu
|
|
ENST00000695655.1:c.2676C>G
|
ENSP00000512086.1:n.2676C>G
|
|
ENST00000695692.1:n.3099C>G
|
|
|
ENST00000245907.11:c.3735C>G
MANE Select
|
ENSP00000245907.4:p.Asp1245Glu
|
|
ENST00000245907.10:c.3735C>G
|
ENSP00000245907.4:p.Asp1245Glu
|
|
ENST00000596238.1:n.178C>G
|
|
|
ENST00000601008.1:c.241+547C>G
|
ENSP00000471384.1:n.241+547C>G
|
|
NM_000064.3:c.3735C>G
|
NP_000055.2:p.Asp1245Glu
|
|
NM_000064.4:c.3735C>G
MANE Select
|
NP_000055.2:p.Asp1245Glu
|
|