ENST00000695651.1:n.2682T>C
|
|
|
ENST00000695653.1:c.2243T>C
|
ENSP00000512084.1:p.Ile748Thr
|
|
ENST00000695654.1:c.3359T>C
|
ENSP00000512085.1:p.Ile1120Thr
|
|
ENST00000695689.1:c.305T>C
|
ENSP00000512101.1:n.305T>C
|
|
ENST00000695690.1:n.525T>C
|
|
|
ENST00000695691.1:n.525T>C
|
|
|
ENST00000245907.11:c.4334T>C
MANE Select
|
ENSP00000245907.4:p.Ile1445Thr
|
|
ENST00000245907.10:c.4334T>C
|
ENSP00000245907.4:p.Ile1445Thr
|
|
ENST00000596548.1:c.455T>C
|
ENSP00000469744.1:p.Ile152Thr
|
|
ENST00000599899.5:n.1293T>C
|
|
|
ENST00000601008.1:c.242-3999T>C
|
ENSP00000471384.1:n.242-3999T>C
|
|
NM_000064.3:c.4334T>C
|
NP_000055.2:p.Ile1445Thr
|
|
NM_000064.4:c.4334T>C
MANE Select
|
NP_000055.2:p.Ile1445Thr
|
|