ENST00000695651.1:n.2671G>A
|
|
|
ENST00000695653.1:c.2232G>A
|
ENSP00000512084.1:p.Arg744=
|
|
ENST00000695654.1:c.3348G>A
|
ENSP00000512085.1:p.Arg1116=
|
|
ENST00000695689.1:c.294G>A
|
ENSP00000512101.1:n.294G>A
|
|
ENST00000695690.1:n.514G>A
|
|
|
ENST00000695691.1:n.514G>A
|
|
|
ENST00000245907.11:c.4323G>A
MANE Select
|
ENSP00000245907.4:p.Arg1441=
|
|
ENST00000245907.10:c.4323G>A
|
ENSP00000245907.4:p.Arg1441=
|
|
ENST00000596548.1:c.444G>A
|
ENSP00000469744.1:p.Arg148=
|
|
ENST00000599899.5:n.1282G>A
|
|
|
ENST00000601008.1:c.242-4010G>A
|
ENSP00000471384.1:n.242-4010G>A
|
|
NM_000064.3:c.4323G>A
|
NP_000055.2:p.Arg1441=
|
|
NM_000064.4:c.4323G>A
MANE Select
|
NP_000055.2:p.Arg1441=
|
|