ENST00000695651.1:n.2304T>G
|
|
|
ENST00000695653.1:c.1865T>G
|
ENSP00000512084.1:p.Leu622Arg
|
|
ENST00000695654.1:c.2981T>G
|
ENSP00000512085.1:p.Leu994Arg
|
|
ENST00000695690.1:n.147T>G
|
|
|
ENST00000695691.1:n.147T>G
|
|
|
ENST00000245907.11:c.3956T>G
MANE Select
|
ENSP00000245907.4:p.Leu1319Arg
|
|
ENST00000245907.10:c.3956T>G
|
ENSP00000245907.4:p.Leu1319Arg
|
|
ENST00000596238.1:n.399T>G
|
|
|
ENST00000596548.1:c.38T>G
|
ENSP00000469744.1:p.Leu13Arg
|
|
ENST00000601008.1:c.241+1745T>G
|
ENSP00000471384.1:n.241+1745T>G
|
|
NM_000064.3:c.3956T>G
|
NP_000055.2:p.Leu1319Arg
|
|
NM_000064.4:c.3956T>G
MANE Select
|
NP_000055.2:p.Leu1319Arg
|
|