ENST00000695901.1:c.798+723T>A
|
ENSP00000512251.1:n.798+723T>A
|
|
ENST00000695911.1:c.846T>A
|
ENSP00000512262.1:n.846T>A
|
|
ENST00000695912.1:c.1065T>A
|
ENSP00000512263.1:p.Thr355=
|
|
ENST00000695913.1:c.*1821T>A
|
ENSP00000512264.1:n.*1821T>A
|
|
ENST00000695914.1:c.828T>A
|
ENSP00000512265.1:p.Thr276=
|
|
ENST00000695918.1:n.296T>A
|
|
|
ENST00000306721.8:c.1068T>A
MANE Select
|
ENSP00000306968.3:p.Thr356=
|
|
ENST00000306721.7:c.1068T>A
|
ENSP00000306968.3:p.Thr356=
|
|
ENST00000347703.7:c.831T>A
|
ENSP00000272789.4:p.Thr277=
|
|
ENST00000410019.3:c.705T>A
|
ENSP00000386833.3:p.Thr235=
|
|
ENST00000410101.7:c.936T>A
|
ENSP00000386656.3:p.Thr312=
|
|
ENST00000467411.5:n.1768+723T>A
|
|
|
ENST00000496441.5:n.1822T>A
|
|
|
NM_031942.4:c.1068T>A
|
NP_114148.3:p.Thr356=
|
|
NM_145810.2:c.831T>A
|
NP_665809.1:p.Thr277=
|
|
XM_011511957.1:c.987T>A
|
XP_011510259.1:p.Thr329=
|
|
XR_923034.1:n.1966T>A
|
|
|
NM_031942.5:c.1068T>A
MANE Select
|
NP_114148.3:p.Thr356=
|
|
NM_145810.3:c.831T>A
|
NP_665809.1:p.Thr277=
|
|