ENST00000700029.2:c.1013_1014delinsTT
|
ENSP00000514759.2:p.Glu338Val
|
|
ENST00000710265.1:c.920_921delinsTT
|
ENSP00000518161.1:p.Glu307Val
|
|
ENST00000472832.3:c.920_921delinsTT
|
ENSP00000483066.2:p.Glu307Val
|
|
ENST00000688158.2:n.1655_1656delinsTT
|
|
|
ENST00000688922.2:c.*750_*751delinsTT
|
ENSP00000508742.2:n.*750_*751delinsTT
|
|
ENST00000700021.1:c.875_876delinsTT
|
ENSP00000514757.1:p.Glu292Val
|
|
ENST00000700022.1:c.*259_*260delinsTT
|
ENSP00000514758.1:n.*259_*260delinsTT
|
|
ENST00000700023.1:n.2078_2079delinsTT
|
|
|
ENST00000700024.1:n.2312_2313delinsTT
|
|
|
ENST00000700025.1:n.1689_1690delinsTT
|
|
|
ENST00000700026.1:n.557_558delinsTT
|
|
|
ENST00000706954.1:c.920_921delinsTT
|
ENSP00000516674.1:p.Glu307Val
|
|
ENST00000706955.1:c.*955_*956delinsTT
|
ENSP00000516675.1:n.*955_*956delinsTT
|
|
ENST00000686459.1:c.*506_*507delinsTT
|
ENSP00000508909.1:n.*506_*507delinsTT
|
|
ENST00000688158.1:c.*1031_*1032delinsTT
|
ENSP00000509254.1:n.*1031_*1032delinsTT
|
|
ENST00000688308.1:c.920_921delinsTT
|
ENSP00000508752.1:p.Glu307Val
|
|
ENST00000688922.1:c.841_842delinsTT
|
|
|
ENST00000693560.1:c.1439_1440delinsTT
|
ENSP00000509861.1:p.Glu480Val
|
|
ENST00000371953.8:c.920_921delinsTT
MANE Select
|
ENSP00000361021.3:p.Glu307Val
|
|
ENST00000371953.7:c.920_921delinsTT
|
ENSP00000361021.3:p.Glu307Val
|
|
ENST00000472832.2:c.347_348delinsTT
|
ENSP00000483066.1:p.Glu116Val
|
|
NM_000314.5:c.920_921delinsTT
|
NP_000305.3:p.Glu307Val
|
|
NM_000314.6:c.920_921delinsTT
|
NP_000305.3:p.Glu307Val
|
|
NM_001304717.2:c.1439_1440delinsTT
|
NP_001291646.2:p.Glu480Val
|
|
NM_001304718.1:c.329_330delinsTT
|
NP_001291647.1:p.Glu110Val
|
|
XM_006717926.2:c.875_876delinsTT
|
XP_006717989.1:p.Glu292Val
|
|
XM_011539981.1:c.920_921delinsTT
|
XP_011538283.1:p.Glu307Val
|
|
XM_011539982.1:c.824_825delinsTT
|
XP_011538284.1:p.Glu275Val
|
|
XR_945791.1:n.1490_1491delinsTT
|
|
|
NM_000314.7:c.920_921delinsTT
|
NP_000305.3:p.Glu307Val
|
|
NM_001304717.5:c.1439_1440delinsTT
|
NP_001291646.4:p.Glu480Val
|
|
NM_001304718.2:c.329_330delinsTT
|
NP_001291647.1:p.Glu110Val
|
|
NM_000314.8:c.920_921delinsTT
MANE Select
|
NP_000305.3:p.Glu307Val
|
|