ENST00000695901.1:c.799-755G=
|
ENSP00000512251.1:n.799-755G=
|
|
ENST00000695911.1:c.926G=
|
ENSP00000512262.1:n.926G=
|
|
ENST00000695912.1:c.1145G=
|
ENSP00000512263.1:p.Arg382=
|
|
ENST00000695913.1:c.*1901G=
|
ENSP00000512264.1:n.*1901G=
|
|
ENST00000695914.1:c.908G=
|
ENSP00000512265.1:p.Arg303=
|
|
ENST00000695918.1:n.376G=
|
|
|
ENST00000306721.8:c.1148G=
MANE Select
|
ENSP00000306968.3:p.Arg383=
|
|
ENST00000306721.7:c.1148G=
|
ENSP00000306968.3:p.Arg383=
|
|
ENST00000347703.7:c.911G=
|
ENSP00000272789.4:p.Arg304=
|
|
ENST00000410019.3:c.785G=
|
ENSP00000386833.3:p.Arg262=
|
|
ENST00000410101.7:c.1016G=
|
ENSP00000386656.3:p.Arg339=
|
|
ENST00000467411.5:n.1769-755G=
|
|
|
ENST00000496441.5:n.1902G=
|
|
|
NM_031942.4:c.1148G=
|
NP_114148.3:p.Arg383=
|
|
NM_145810.2:c.911G=
|
NP_665809.1:p.Arg304=
|
|
XM_011511957.1:c.1067G=
|
XP_011510259.1:p.Arg356=
|
|
XR_923034.1:n.2046G=
|
|
|
NM_031942.5:c.1148G=
MANE Select
|
NP_114148.3:p.Arg383=
|
|
NM_145810.3:c.911G=
|
NP_665809.1:p.Arg304=
|
|