ENST00000695651.1:n.2058T>G
|
|
|
ENST00000695652.1:c.3587T>G
|
ENSP00000512083.1:p.Leu1196Arg
|
|
ENST00000695653.1:c.1619T>G
|
ENSP00000512084.1:p.Leu540Arg
|
|
ENST00000695654.1:c.2735T>G
|
ENSP00000512085.1:p.Leu912Arg
|
|
ENST00000695655.1:c.2651T>G
|
ENSP00000512086.1:n.2651T>G
|
|
ENST00000695692.1:n.3074T>G
|
|
|
ENST00000245907.11:c.3710T>G
MANE Select
|
ENSP00000245907.4:p.Leu1237Arg
|
|
ENST00000245907.10:c.3710T>G
|
ENSP00000245907.4:p.Leu1237Arg
|
|
ENST00000596238.1:n.153T>G
|
|
|
ENST00000601008.1:c.241+522T>G
|
ENSP00000471384.1:n.241+522T>G
|
|
NM_000064.3:c.3710T>G
|
NP_000055.2:p.Leu1237Arg
|
|
NM_000064.4:c.3710T>G
MANE Select
|
NP_000055.2:p.Leu1237Arg
|
|