ENST00000695651.1:n.2069C>G
|
|
|
ENST00000695652.1:c.3598C>G
|
ENSP00000512083.1:p.Leu1200Val
|
|
ENST00000695653.1:c.1630C>G
|
ENSP00000512084.1:p.Leu544Val
|
|
ENST00000695654.1:c.2746C>G
|
ENSP00000512085.1:p.Leu916Val
|
|
ENST00000695655.1:c.2662C>G
|
ENSP00000512086.1:n.2662C>G
|
|
ENST00000695692.1:n.3085C>G
|
|
|
ENST00000245907.11:c.3721C>G
MANE Select
|
ENSP00000245907.4:p.Leu1241Val
|
|
ENST00000245907.10:c.3721C>G
|
ENSP00000245907.4:p.Leu1241Val
|
|
ENST00000596238.1:n.164C>G
|
|
|
ENST00000601008.1:c.241+533C>G
|
ENSP00000471384.1:n.241+533C>G
|
|
NM_000064.3:c.3721C>G
|
NP_000055.2:p.Leu1241Val
|
|
NM_000064.4:c.3721C>G
MANE Select
|
NP_000055.2:p.Leu1241Val
|
|