ENST00000695651.1:n.794T>G
|
|
|
ENST00000695652.1:c.2323T>G
|
ENSP00000512083.1:p.Cys775Gly
|
|
ENST00000695653.1:c.355T>G
|
ENSP00000512084.1:p.Cys119Gly
|
|
ENST00000695654.1:c.1570T>G
|
ENSP00000512085.1:p.Cys524Gly
|
|
ENST00000695655.1:c.1387T>G
|
ENSP00000512086.1:n.1387T>G
|
|
ENST00000695692.1:n.1810T>G
|
|
|
ENST00000245907.11:c.2446T>G
MANE Select
|
ENSP00000245907.4:p.Cys816Gly
|
|
ENST00000245907.10:c.2446T>G
|
ENSP00000245907.4:p.Cys816Gly
|
|
ENST00000602053.1:n.494T>G
|
|
|
NM_000064.3:c.2446T>G
|
NP_000055.2:p.Cys816Gly
|
|
NM_000064.4:c.2446T>G
MANE Select
|
NP_000055.2:p.Cys816Gly
|
|