ENST00000695651.1:n.1100C>G
|
|
|
ENST00000695652.1:c.2629C>G
|
ENSP00000512083.1:p.His877Asp
|
|
ENST00000695653.1:c.661C>G
|
ENSP00000512084.1:p.His221Asp
|
|
ENST00000695654.1:c.1876C>G
|
ENSP00000512085.1:p.His626Asp
|
|
ENST00000695655.1:c.1693C>G
|
ENSP00000512086.1:n.1693C>G
|
|
ENST00000695692.1:n.2116C>G
|
|
|
ENST00000245907.11:c.2752C>G
MANE Select
|
ENSP00000245907.4:p.His918Asp
|
|
ENST00000245907.10:c.2752C>G
|
ENSP00000245907.4:p.His918Asp
|
|
ENST00000594005.1:n.328C>G
|
|
|
NM_000064.3:c.2752C>G
|
NP_000055.2:p.His918Asp
|
|
NM_000064.4:c.2752C>G
MANE Select
|
NP_000055.2:p.His918Asp
|
|