ENST00000695651.1:n.2844A>G
|
|
|
ENST00000695653.1:c.2405A>G
|
ENSP00000512084.1:p.Asp802Gly
|
|
ENST00000695654.1:c.3521A>G
|
ENSP00000512085.1:p.Asp1174Gly
|
|
ENST00000695689.1:c.467A>G
|
ENSP00000512101.1:n.467A>G
|
|
ENST00000695690.1:n.1561A>G
|
|
|
ENST00000695691.1:n.1357A>G
|
|
|
ENST00000245907.11:c.4496A>G
MANE Select
|
ENSP00000245907.4:p.Asp1499Gly
|
|
ENST00000245907.10:c.4496A>G
|
ENSP00000245907.4:p.Asp1499Gly
|
|
ENST00000599668.1:n.91A>G
|
|
|
ENST00000599899.5:n.1455A>G
|
|
|
ENST00000601008.1:c.242-1499A>G
|
ENSP00000471384.1:n.242-1499A>G
|
|
NM_000064.3:c.4496A>G
|
NP_000055.2:p.Asp1499Gly
|
|
NM_000064.4:c.4496A>G
MANE Select
|
NP_000055.2:p.Asp1499Gly
|
|