ENST00000695651.1:n.2028T>G
|
|
|
ENST00000695652.1:c.3557T>G
|
ENSP00000512083.1:p.Leu1186Arg
|
|
ENST00000695653.1:c.1589T>G
|
ENSP00000512084.1:p.Leu530Arg
|
|
ENST00000695654.1:c.2705T>G
|
ENSP00000512085.1:p.Leu902Arg
|
|
ENST00000695655.1:c.2621T>G
|
ENSP00000512086.1:n.2621T>G
|
|
ENST00000695692.1:n.3044T>G
|
|
|
ENST00000245907.11:c.3680T>G
MANE Select
|
ENSP00000245907.4:p.Leu1227Arg
|
|
ENST00000245907.10:c.3680T>G
|
ENSP00000245907.4:p.Leu1227Arg
|
|
ENST00000596238.1:n.123T>G
|
|
|
ENST00000601008.1:c.241+492T>G
|
ENSP00000471384.1:n.241+492T>G
|
|
NM_000064.3:c.3680T>G
|
NP_000055.2:p.Leu1227Arg
|
|
NM_000064.4:c.3680T>G
MANE Select
|
NP_000055.2:p.Leu1227Arg
|
|