ENST00000695901.1:c.799-755G>T
|
ENSP00000512251.1:n.799-755G>T
|
|
ENST00000695911.1:c.926G>T
|
ENSP00000512262.1:n.926G>T
|
|
ENST00000695912.1:c.1145G>T
|
ENSP00000512263.1:p.Arg382Leu
|
|
ENST00000695913.1:c.*1901G>T
|
ENSP00000512264.1:n.*1901G>T
|
|
ENST00000695914.1:c.908G>T
|
ENSP00000512265.1:p.Arg303Leu
|
|
ENST00000695918.1:n.376G>T
|
|
|
ENST00000306721.8:c.1148G>T
MANE Select
|
ENSP00000306968.3:p.Arg383Leu
|
|
ENST00000306721.7:c.1148G>T
|
ENSP00000306968.3:p.Arg383Leu
|
|
ENST00000347703.7:c.911G>T
|
ENSP00000272789.4:p.Arg304Leu
|
|
ENST00000410019.3:c.785G>T
|
ENSP00000386833.3:p.Arg262Leu
|
|
ENST00000410101.7:c.1016G>T
|
ENSP00000386656.3:p.Arg339Leu
|
|
ENST00000467411.5:n.1769-755G>T
|
|
|
ENST00000496441.5:n.1902G>T
|
|
|
NM_031942.4:c.1148G>T
|
NP_114148.3:p.Arg383Leu
|
|
NM_145810.2:c.911G>T
|
NP_665809.1:p.Arg304Leu
|
|
XM_011511957.1:c.1067G>T
|
XP_011510259.1:p.Arg356Leu
|
|
XR_923034.1:n.2046G>T
|
|
|
NM_031942.5:c.1148G>T
MANE Select
|
NP_114148.3:p.Arg383Leu
|
|
NM_145810.3:c.911G>T
|
NP_665809.1:p.Arg304Leu
|
|