ENST00000695651.1:n.2006T>G
|
|
|
ENST00000695652.1:c.3535T>G
|
ENSP00000512083.1:p.Trp1179Gly
|
|
ENST00000695653.1:c.1567T>G
|
ENSP00000512084.1:p.Trp523Gly
|
|
ENST00000695654.1:c.2683T>G
|
ENSP00000512085.1:p.Trp895Gly
|
|
ENST00000695655.1:c.2599T>G
|
ENSP00000512086.1:n.2599T>G
|
|
ENST00000695692.1:n.3022T>G
|
|
|
ENST00000245907.11:c.3658T>G
MANE Select
|
ENSP00000245907.4:p.Trp1220Gly
|
|
ENST00000245907.10:c.3658T>G
|
ENSP00000245907.4:p.Trp1220Gly
|
|
ENST00000596238.1:n.101T>G
|
|
|
ENST00000601008.1:c.241+470T>G
|
ENSP00000471384.1:n.241+470T>G
|
|
NM_000064.3:c.3658T>G
|
NP_000055.2:p.Trp1220Gly
|
|
NM_000064.4:c.3658T>G
MANE Select
|
NP_000055.2:p.Trp1220Gly
|
|