ENST00000695901.1:c.799-747G>T
|
ENSP00000512251.1:n.799-747G>T
|
|
ENST00000695911.1:c.934G>T
|
ENSP00000512262.1:n.934G>T
|
|
ENST00000695912.1:c.1153G>T
|
ENSP00000512263.1:p.Glu385Ter
|
|
ENST00000695913.1:c.*1909G>T
|
ENSP00000512264.1:n.*1909G>T
|
|
ENST00000695914.1:c.916G>T
|
ENSP00000512265.1:p.Glu306Ter
|
|
ENST00000695918.1:n.384G>T
|
|
|
ENST00000306721.8:c.1156G>T
MANE Select
|
ENSP00000306968.3:p.Glu386Ter
|
|
ENST00000306721.7:c.1156G>T
|
ENSP00000306968.3:p.Glu386Ter
|
|
ENST00000347703.7:c.919G>T
|
ENSP00000272789.4:p.Glu307Ter
|
|
ENST00000410019.3:c.793G>T
|
ENSP00000386833.3:p.Glu265Ter
|
|
ENST00000410101.7:c.1024G>T
|
ENSP00000386656.3:p.Glu342Ter
|
|
ENST00000467411.5:n.1769-747G>T
|
|
|
ENST00000496441.5:n.1910G>T
|
|
|
NM_031942.4:c.1156G>T
|
NP_114148.3:p.Glu386Ter
|
|
NM_145810.2:c.919G>T
|
NP_665809.1:p.Glu307Ter
|
|
XM_011511957.1:c.1075G>T
|
XP_011510259.1:p.Glu359Ter
|
|
XR_923034.1:n.2054G>T
|
|
|
NM_031942.5:c.1156G>T
MANE Select
|
NP_114148.3:p.Glu386Ter
|
|
NM_145810.3:c.919G>T
|
NP_665809.1:p.Glu307Ter
|
|