ENST00000235329.10:c.2124G>C
MANE Select
|
ENSP00000235329.5:p.Glu708Asp
|
|
ENST00000674548.1:c.2124G>C
|
ENSP00000502185.1:p.Glu708Asp
|
|
ENST00000674658.1:c.1779G>C
|
ENSP00000502334.1:p.Glu593Asp
|
|
ENST00000674817.1:c.2124G>C
|
ENSP00000502151.1:p.Glu708Asp
|
|
ENST00000674910.1:c.2124G>C
|
ENSP00000501716.1:p.Glu708Asp
|
|
ENST00000675043.1:n.92G>C
|
|
|
ENST00000675053.1:c.2124G>C
|
ENSP00000501646.1:p.Glu708Asp
|
|
ENST00000675113.1:c.2124G>C
|
ENSP00000502623.1:p.Glu708Asp
|
|
ENST00000675231.1:c.2124G>C
|
ENSP00000502404.1:p.Glu708Asp
|
|
ENST00000675298.1:c.2124G>C
|
ENSP00000501839.1:p.Glu708Asp
|
|
ENST00000675404.1:n.2359G>C
|
|
|
ENST00000675483.1:n.2252G>C
|
|
|
ENST00000675512.1:c.*2126G>C
|
ENSP00000502630.1:n.*2126G>C
|
|
ENST00000675528.1:n.1615G>C
|
|
|
ENST00000675817.1:c.2256G>C
|
ENSP00000502422.1:p.Glu752Asp
|
|
ENST00000675872.1:n.2484G>C
|
|
|
ENST00000675919.1:c.2124G>C
|
ENSP00000501776.1:p.Glu708Asp
|
|
ENST00000675959.1:n.2630G>C
|
|
|
ENST00000675987.1:c.*97G>C
|
ENSP00000502145.1:n.*97G>C
|
|
ENST00000676293.1:c.2124G>C
|
ENSP00000502362.1:p.Glu708Asp
|
|
ENST00000676295.1:n.537G>C
|
|
|
ENST00000676426.1:c.*1124G>C
|
ENSP00000502359.1:n.*1124G>C
|
|
ENST00000235329.9:c.2124G>C
|
ENSP00000235329.5:p.Glu708Asp
|
|
ENST00000444836.5:c.2124G>C
|
ENSP00000416338.1:p.Glu708Asp
|
|
NM_001127660.1:c.2124G>C
|
NP_001121132.1:p.Glu708Asp
|
|
NM_014874.3:c.2124G>C , LRG_255t1:c.2124G>C
|
NP_055689.1:p.Glu708Asp
|
|
XM_005263543.2:c.2124G>C
|
XP_005263600.1:p.Glu708Asp
|
|
XM_005263545.2:c.2124G>C
|
XP_005263602.1:p.Glu708Asp
|
|
XM_005263547.2:c.2124G>C
|
XP_005263604.1:p.Glu708Asp
|
|
XM_005263548.2:c.2124G>C
|
XP_005263605.1:p.Glu708Asp
|
|
XM_005263543.3:c.2124G>C
|
XP_005263600.1:p.Glu708Asp
|
|
XM_005263545.3:c.2124G>C
|
XP_005263602.1:p.Glu708Asp
|
|
XM_005263547.3:c.2124G>C
|
XP_005263604.1:p.Glu708Asp
|
|
XM_005263548.3:c.2124G>C
|
XP_005263605.1:p.Glu708Asp
|
|
XM_024451299.1:c.2124G>C
|
XP_024307067.1:p.Glu708Asp
|
|
NM_014874.4:c.2124G>C
MANE Select
|
NP_055689.1:p.Glu708Asp
|
|
NM_001127660.2:c.2124G>C
|
NP_001121132.1:p.Glu708Asp
|
|