ENST00000695651.1:n.2111T>G
|
|
|
ENST00000695652.1:c.3640T>G
|
ENSP00000512083.1:p.Trp1214Gly
|
|
ENST00000695653.1:c.1672T>G
|
ENSP00000512084.1:p.Trp558Gly
|
|
ENST00000695654.1:c.2788T>G
|
ENSP00000512085.1:p.Trp930Gly
|
|
ENST00000695655.1:c.2704T>G
|
ENSP00000512086.1:n.2704T>G
|
|
ENST00000695692.1:n.3127T>G
|
|
|
ENST00000245907.11:c.3763T>G
MANE Select
|
ENSP00000245907.4:p.Trp1255Gly
|
|
ENST00000245907.10:c.3763T>G
|
ENSP00000245907.4:p.Trp1255Gly
|
|
ENST00000596238.1:n.206T>G
|
|
|
ENST00000601008.1:c.241+575T>G
|
ENSP00000471384.1:n.241+575T>G
|
|
NM_000064.3:c.3763T>G
|
NP_000055.2:p.Trp1255Gly
|
|
NM_000064.4:c.3763T>G
MANE Select
|
NP_000055.2:p.Trp1255Gly
|
|