ENST00000695651.1:n.2059C>G
|
|
|
ENST00000695652.1:c.3588C>G
|
ENSP00000512083.1:p.Leu1196=
|
|
ENST00000695653.1:c.1620C>G
|
ENSP00000512084.1:p.Leu540=
|
|
ENST00000695654.1:c.2736C>G
|
ENSP00000512085.1:p.Leu912=
|
|
ENST00000695655.1:c.2652C>G
|
ENSP00000512086.1:n.2652C>G
|
|
ENST00000695692.1:n.3075C>G
|
|
|
ENST00000245907.11:c.3711C>G
MANE Select
|
ENSP00000245907.4:p.Leu1237=
|
|
ENST00000245907.10:c.3711C>G
|
ENSP00000245907.4:p.Leu1237=
|
|
ENST00000596238.1:n.154C>G
|
|
|
ENST00000601008.1:c.241+523C>G
|
ENSP00000471384.1:n.241+523C>G
|
|
NM_000064.3:c.3711C>G
|
NP_000055.2:p.Leu1237=
|
|
NM_000064.4:c.3711C>G
MANE Select
|
NP_000055.2:p.Leu1237=
|
|