ENST00000695651.1:n.2667A>G
|
|
|
ENST00000695653.1:c.2228A>G
|
ENSP00000512084.1:p.Asp743Gly
|
|
ENST00000695654.1:c.3344A>G
|
ENSP00000512085.1:p.Asp1115Gly
|
|
ENST00000695689.1:c.290A>G
|
ENSP00000512101.1:n.290A>G
|
|
ENST00000695690.1:n.510A>G
|
|
|
ENST00000695691.1:n.510A>G
|
|
|
ENST00000245907.11:c.4319A>G
MANE Select
|
ENSP00000245907.4:p.Asp1440Gly
|
|
ENST00000245907.10:c.4319A>G
|
ENSP00000245907.4:p.Asp1440Gly
|
|
ENST00000596548.1:c.440A>G
|
ENSP00000469744.1:p.Asp147Gly
|
|
ENST00000599899.5:n.1278A>G
|
|
|
ENST00000601008.1:c.242-4014A>G
|
ENSP00000471384.1:n.242-4014A>G
|
|
NM_000064.3:c.4319A>G
|
NP_000055.2:p.Asp1440Gly
|
|
NM_000064.4:c.4319A>G
MANE Select
|
NP_000055.2:p.Asp1440Gly
|
|