ENST00000695651.1:n.2563A>C
|
|
|
ENST00000695653.1:c.2124A>C
|
ENSP00000512084.1:p.Ile708=
|
|
ENST00000695654.1:c.3240A>C
|
ENSP00000512085.1:p.Ile1080=
|
|
ENST00000695689.1:c.186A>C
|
ENSP00000512101.1:n.186A>C
|
|
ENST00000695690.1:n.406A>C
|
|
|
ENST00000695691.1:n.406A>C
|
|
|
ENST00000245907.11:c.4215A>C
MANE Select
|
ENSP00000245907.4:p.Ile1405=
|
|
ENST00000245907.10:c.4215A>C
|
ENSP00000245907.4:p.Ile1405=
|
|
ENST00000596548.1:c.336A>C
|
ENSP00000469744.1:p.Ile112=
|
|
ENST00000599899.5:n.1174A>C
|
|
|
ENST00000601008.1:c.242-4229A>C
|
ENSP00000471384.1:n.242-4229A>C
|
|
NM_000064.3:c.4215A>C
|
NP_000055.2:p.Ile1405=
|
|
NM_000064.4:c.4215A>C
MANE Select
|
NP_000055.2:p.Ile1405=
|
|