|
ENST00000700029.2:c.1014G>T
|
ENSP00000514759.2:p.Glu338Asp
|
|
|
ENST00000710265.1:c.921G>T
|
ENSP00000518161.1:p.Glu307Asp
|
|
|
ENST00000472832.3:c.921G>T
|
ENSP00000483066.2:p.Glu307Asp
|
|
|
ENST00000688158.2:n.1656G>T
|
|
|
|
ENST00000688922.2:c.*751G>T
|
ENSP00000508742.2:n.*751G>T
|
|
|
ENST00000700021.1:c.876G>T
|
ENSP00000514757.1:p.Glu292Asp
|
|
|
ENST00000700022.1:c.*260G>T
|
ENSP00000514758.1:n.*260G>T
|
|
|
ENST00000700023.1:n.2079G>T
|
|
|
|
ENST00000700024.1:n.2313G>T
|
|
|
|
ENST00000700025.1:n.1690G>T
|
|
|
|
ENST00000700026.1:n.558G>T
|
|
|
|
ENST00000706954.1:c.921G>T
|
ENSP00000516674.1:p.Glu307Asp
|
|
|
ENST00000706955.1:c.*956G>T
|
ENSP00000516675.1:n.*956G>T
|
|
|
ENST00000686459.1:c.*507G>T
|
ENSP00000508909.1:n.*507G>T
|
|
|
ENST00000688158.1:c.*1032G>T
|
ENSP00000509254.1:n.*1032G>T
|
|
|
ENST00000688308.1:c.921G>T
|
ENSP00000508752.1:p.Glu307Asp
|
|
|
ENST00000688922.1:c.842G>T
|
|
|
|
ENST00000693560.1:c.1440G>T
|
ENSP00000509861.1:p.Glu480Asp
|
|
|
ENST00000371953.8:c.921G>T
MANE Select
|
ENSP00000361021.3:p.Glu307Asp
|
|
|
ENST00000371953.7:c.921G>T
|
ENSP00000361021.3:p.Glu307Asp
|
|
|
ENST00000472832.2:c.348G>T
|
ENSP00000483066.1:p.Glu116Asp
|
|
|
NM_000314.5:c.921G>T
|
NP_000305.3:p.Glu307Asp
|
|
|
NM_000314.6:c.921G>T
|
NP_000305.3:p.Glu307Asp
|
|
|
NM_001304717.2:c.1440G>T
|
NP_001291646.2:p.Glu480Asp
|
|
|
NM_001304718.1:c.330G>T
|
NP_001291647.1:p.Glu110Asp
|
|
|
XM_006717926.2:c.876G>T
|
XP_006717989.1:p.Glu292Asp
|
|
|
XM_011539981.1:c.921G>T
|
XP_011538283.1:p.Glu307Asp
|
|
|
XM_011539982.1:c.825G>T
|
XP_011538284.1:p.Glu275Asp
|
|
|
XR_945791.1:n.1491G>T
|
|
|
|
NM_000314.7:c.921G>T
|
NP_000305.3:p.Glu307Asp
|
|
|
NM_001304717.5:c.1440G>T
|
NP_001291646.4:p.Glu480Asp
|
|
|
NM_001304718.2:c.330G>T
|
NP_001291647.1:p.Glu110Asp
|
|
|
NM_000314.8:c.921G>T
MANE Select
|
NP_000305.3:p.Glu307Asp
|
|
