ENST00000695651.1:n.2272C>A
|
|
|
ENST00000695653.1:c.1833C>A
|
ENSP00000512084.1:p.Thr611=
|
|
ENST00000695654.1:c.2949C>A
|
ENSP00000512085.1:p.Thr983=
|
|
ENST00000695690.1:n.115C>A
|
|
|
ENST00000695691.1:n.115C>A
|
|
|
ENST00000245907.11:c.3924C>A
MANE Select
|
ENSP00000245907.4:p.Thr1308=
|
|
ENST00000245907.10:c.3924C>A
|
ENSP00000245907.4:p.Thr1308=
|
|
ENST00000596238.1:n.367C>A
|
|
|
ENST00000596548.1:c.6C>A
|
ENSP00000469744.1:p.Thr2=
|
|
ENST00000601008.1:c.241+1713C>A
|
ENSP00000471384.1:n.241+1713C>A
|
|
NM_000064.3:c.3924C>A
|
NP_000055.2:p.Thr1308=
|
|
NM_000064.4:c.3924C>A
MANE Select
|
NP_000055.2:p.Thr1308=
|
|