ENST00000695901.1:c.799-744G>T
|
ENSP00000512251.1:n.799-744G>T
|
|
ENST00000695911.1:c.937G>T
|
ENSP00000512262.1:n.937G>T
|
|
ENST00000695912.1:c.1156G>T
|
ENSP00000512263.1:p.Glu386Ter
|
|
ENST00000695913.1:c.*1912G>T
|
ENSP00000512264.1:n.*1912G>T
|
|
ENST00000695914.1:c.919G>T
|
ENSP00000512265.1:p.Glu307Ter
|
|
ENST00000695918.1:n.387G>T
|
|
|
ENST00000306721.8:c.1159G>T
MANE Select
|
ENSP00000306968.3:p.Glu387Ter
|
|
ENST00000306721.7:c.1159G>T
|
ENSP00000306968.3:p.Glu387Ter
|
|
ENST00000347703.7:c.922G>T
|
ENSP00000272789.4:p.Glu308Ter
|
|
ENST00000410019.3:c.796G>T
|
ENSP00000386833.3:p.Glu266Ter
|
|
ENST00000410101.7:c.1027G>T
|
ENSP00000386656.3:p.Glu343Ter
|
|
ENST00000467411.5:n.1769-744G>T
|
|
|
ENST00000496441.5:n.1913G>T
|
|
|
NM_031942.4:c.1159G>T
|
NP_114148.3:p.Glu387Ter
|
|
NM_145810.2:c.922G>T
|
NP_665809.1:p.Glu308Ter
|
|
XM_011511957.1:c.1078G>T
|
XP_011510259.1:p.Glu360Ter
|
|
XR_923034.1:n.2057G>T
|
|
|
NM_031942.5:c.1159G>T
MANE Select
|
NP_114148.3:p.Glu387Ter
|
|
NM_145810.3:c.922G>T
|
NP_665809.1:p.Glu308Ter
|
|