ENST00000695901.1:c.799-777T>A
|
ENSP00000512251.1:n.799-777T>A
|
|
ENST00000695911.1:c.904T>A
|
ENSP00000512262.1:n.904T>A
|
|
ENST00000695912.1:c.1123T>A
|
ENSP00000512263.1:p.Cys375Ser
|
|
ENST00000695913.1:c.*1879T>A
|
ENSP00000512264.1:n.*1879T>A
|
|
ENST00000695914.1:c.886T>A
|
ENSP00000512265.1:p.Cys296Ser
|
|
ENST00000695918.1:n.354T>A
|
|
|
ENST00000306721.8:c.1126T>A
MANE Select
|
ENSP00000306968.3:p.Cys376Ser
|
|
ENST00000306721.7:c.1126T>A
|
ENSP00000306968.3:p.Cys376Ser
|
|
ENST00000347703.7:c.889T>A
|
ENSP00000272789.4:p.Cys297Ser
|
|
ENST00000410019.3:c.763T>A
|
ENSP00000386833.3:p.Cys255Ser
|
|
ENST00000410101.7:c.994T>A
|
ENSP00000386656.3:p.Cys332Ser
|
|
ENST00000467411.5:n.1769-777T>A
|
|
|
ENST00000496441.5:n.1880T>A
|
|
|
NM_031942.4:c.1126T>A
|
NP_114148.3:p.Cys376Ser
|
|
NM_145810.2:c.889T>A
|
NP_665809.1:p.Cys297Ser
|
|
XM_011511957.1:c.1045T>A
|
XP_011510259.1:p.Cys349Ser
|
|
XR_923034.1:n.2024T>A
|
|
|
NM_031942.5:c.1126T>A
MANE Select
|
NP_114148.3:p.Cys376Ser
|
|
NM_145810.3:c.889T>A
|
NP_665809.1:p.Cys297Ser
|
|