ENST00000695651.1:n.2084T>G
|
|
|
ENST00000695652.1:c.3613T>G
|
ENSP00000512083.1:p.Phe1205Val
|
|
ENST00000695653.1:c.1645T>G
|
ENSP00000512084.1:p.Phe549Val
|
|
ENST00000695654.1:c.2761T>G
|
ENSP00000512085.1:p.Phe921Val
|
|
ENST00000695655.1:c.2677T>G
|
ENSP00000512086.1:n.2677T>G
|
|
ENST00000695692.1:n.3100T>G
|
|
|
ENST00000245907.11:c.3736T>G
MANE Select
|
ENSP00000245907.4:p.Phe1246Val
|
|
ENST00000245907.10:c.3736T>G
|
ENSP00000245907.4:p.Phe1246Val
|
|
ENST00000596238.1:n.179T>G
|
|
|
ENST00000601008.1:c.241+548T>G
|
ENSP00000471384.1:n.241+548T>G
|
|
NM_000064.3:c.3736T>G
|
NP_000055.2:p.Phe1246Val
|
|
NM_000064.4:c.3736T>G
MANE Select
|
NP_000055.2:p.Phe1246Val
|
|