ENST00000695651.1:n.2319C>G
|
|
|
ENST00000695653.1:c.1880C>G
|
ENSP00000512084.1:p.Thr627Ser
|
|
ENST00000695654.1:c.2996C>G
|
ENSP00000512085.1:p.Thr999Ser
|
|
ENST00000695690.1:n.162C>G
|
|
|
ENST00000695691.1:n.162C>G
|
|
|
ENST00000245907.11:c.3971C>G
MANE Select
|
ENSP00000245907.4:p.Thr1324Ser
|
|
ENST00000245907.10:c.3971C>G
|
ENSP00000245907.4:p.Thr1324Ser
|
|
ENST00000596238.1:n.414C>G
|
|
|
ENST00000596548.1:c.53C>G
|
ENSP00000469744.1:p.Thr18Ser
|
|
ENST00000601008.1:c.241+1913C>G
|
ENSP00000471384.1:n.241+1913C>G
|
|
NM_000064.3:c.3971C>G
|
NP_000055.2:p.Thr1324Ser
|
|
NM_000064.4:c.3971C>G
MANE Select
|
NP_000055.2:p.Thr1324Ser
|
|