ENST00000695901.1:c.799-754T>A
|
ENSP00000512251.1:n.799-754T>A
|
|
ENST00000695911.1:c.927T>A
|
ENSP00000512262.1:n.927T>A
|
|
ENST00000695912.1:c.1146T>A
|
ENSP00000512263.1:p.Arg382=
|
|
ENST00000695913.1:c.*1902T>A
|
ENSP00000512264.1:n.*1902T>A
|
|
ENST00000695914.1:c.909T>A
|
ENSP00000512265.1:p.Arg303=
|
|
ENST00000695918.1:n.377T>A
|
|
|
ENST00000306721.8:c.1149T>A
MANE Select
|
ENSP00000306968.3:p.Arg383=
|
|
ENST00000306721.7:c.1149T>A
|
ENSP00000306968.3:p.Arg383=
|
|
ENST00000347703.7:c.912T>A
|
ENSP00000272789.4:p.Arg304=
|
|
ENST00000410019.3:c.786T>A
|
ENSP00000386833.3:p.Arg262=
|
|
ENST00000410101.7:c.1017T>A
|
ENSP00000386656.3:p.Arg339=
|
|
ENST00000467411.5:n.1769-754T>A
|
|
|
ENST00000496441.5:n.1903T>A
|
|
|
NM_031942.4:c.1149T>A
|
NP_114148.3:p.Arg383=
|
|
NM_145810.2:c.912T>A
|
NP_665809.1:p.Arg304=
|
|
XM_011511957.1:c.1068T>A
|
XP_011510259.1:p.Arg356=
|
|
XR_923034.1:n.2047T>A
|
|
|
NM_031942.5:c.1149T>A
MANE Select
|
NP_114148.3:p.Arg383=
|
|
NM_145810.3:c.912T>A
|
NP_665809.1:p.Arg304=
|
|