ENST00000695651.1:n.2871A>G
|
|
|
ENST00000695653.1:c.2432A>G
|
ENSP00000512084.1:p.Asp811Gly
|
|
ENST00000695654.1:c.3548A>G
|
ENSP00000512085.1:p.Asp1183Gly
|
|
ENST00000695689.1:c.494A>G
|
ENSP00000512101.1:n.494A>G
|
|
ENST00000695690.1:n.1588A>G
|
|
|
ENST00000695691.1:n.1384A>G
|
|
|
ENST00000245907.11:c.4523A>G
MANE Select
|
ENSP00000245907.4:p.Asp1508Gly
|
|
ENST00000245907.10:c.4523A>G
|
ENSP00000245907.4:p.Asp1508Gly
|
|
ENST00000599668.1:n.118A>G
|
|
|
ENST00000599899.5:n.1482A>G
|
|
|
ENST00000601008.1:c.242-1472A>G
|
ENSP00000471384.1:n.242-1472A>G
|
|
NM_000064.3:c.4523A>G
|
NP_000055.2:p.Asp1508Gly
|
|
NM_000064.4:c.4523A>G
MANE Select
|
NP_000055.2:p.Asp1508Gly
|
|