ENST00000695651.1:n.2665C>G
|
|
|
ENST00000695653.1:c.2226C>G
|
ENSP00000512084.1:p.Ser742=
|
|
ENST00000695654.1:c.3342C>G
|
ENSP00000512085.1:p.Ser1114=
|
|
ENST00000695689.1:c.288C>G
|
ENSP00000512101.1:n.288C>G
|
|
ENST00000695690.1:n.508C>G
|
|
|
ENST00000695691.1:n.508C>G
|
|
|
ENST00000245907.11:c.4317C>G
MANE Select
|
ENSP00000245907.4:p.Ser1439=
|
|
ENST00000245907.10:c.4317C>G
|
ENSP00000245907.4:p.Ser1439=
|
|
ENST00000596548.1:c.438C>G
|
ENSP00000469744.1:p.Ser146=
|
|
ENST00000599899.5:n.1276C>G
|
|
|
ENST00000601008.1:c.242-4016C>G
|
ENSP00000471384.1:n.242-4016C>G
|
|
NM_000064.3:c.4317C>G
|
NP_000055.2:p.Ser1439=
|
|
NM_000064.4:c.4317C>G
MANE Select
|
NP_000055.2:p.Ser1439=
|
|