|
ENST00000260570.8:c.830A>T
MANE Select
|
ENSP00000260570.3:p.Glu277Val
|
|
|
ENST00000476264.7:n.1119A>T
|
|
|
|
ENST00000674701.1:c.830A>T
|
ENSP00000502275.1:p.Glu277Val
|
|
|
ENST00000674824.1:c.767A>T
|
ENSP00000501824.1:p.Glu256Val
|
|
|
ENST00000674932.1:c.*493A>T
|
ENSP00000501967.1:n.*493A>T
|
|
|
ENST00000675410.1:c.149A>T
|
ENSP00000502030.1:p.Glu50Val
|
|
|
ENST00000675618.1:n.910A>T
|
|
|
|
ENST00000675690.1:c.830A>T
|
ENSP00000502283.1:p.Glu277Val
|
|
|
ENST00000675728.1:c.767A>T
|
ENSP00000501700.1:p.Glu256Val
|
|
|
ENST00000675729.1:c.830A>T
|
ENSP00000502319.1:p.Glu277Val
|
|
|
ENST00000675963.1:c.*528A>T
|
ENSP00000502708.1:n.*528A>T
|
|
|
ENST00000676119.1:c.*120A>T
|
ENSP00000501701.1:n.*120A>T
|
|
|
ENST00000676300.1:n.916A>T
|
|
|
|
ENST00000260570.7:c.830A>T
|
ENSP00000260570.3:p.Glu277Val
|
|
|
ENST00000359466.10:c.830A>T
|
ENSP00000352443.6:p.Glu277Val
|
|
|
ENST00000416524.2:c.767A>T
|
ENSP00000407408.2:p.Glu256Val
|
|
|
ENST00000476264.6:n.776A>T
|
|
|
|
ENST00000507184.5:n.962A>T
|
|
|
|
ENST00000511842.5:n.855A>T
|
|
|
|
NM_015662.2:c.830A>T
|
NP_056477.1:p.Glu277Val
|
|
|
XM_005264254.1:c.830A>T
|
XP_005264311.1:p.Glu277Val
|
|
|
XM_006711986.2:c.767A>T
|
XP_006712049.1:p.Glu256Val
|
|
|
XM_006711987.1:c.830A>T
|
XP_006712050.1:p.Glu277Val
|
|
|
XM_011532757.1:c.149A>T
|
XP_011531059.1:p.Glu50Val
|
|
|
XM_011532758.1:c.830A>T
|
XP_011531060.1:p.Glu277Val
|
|
|
XM_006711986.3:c.767A>T
|
XP_006712049.1:p.Glu256Val
|
|
|
XM_011532757.2:c.149A>T
|
XP_011531059.1:p.Glu50Val
|
|
|
XM_017003790.1:c.767A>T
|
XP_016859279.1:p.Glu256Val
|
|
|
XM_017003791.1:c.149A>T
|
XP_016859280.1:p.Glu50Val
|
|
|
XM_017003792.1:c.830A>T
|
XP_016859281.1:p.Glu277Val
|
|
|
XM_017003793.1:c.-621A>T
|
XP_016859282.1:n.-621A>T
|
|
|
XM_017003794.1:c.-621A>T
|
XP_016859283.1:n.-621A>T
|
|
|
XM_017003795.1:c.-993A>T
|
XP_016859284.1:n.-993A>T
|
|
|
XR_001738698.1:n.885A>T
|
|
|
|
NM_015662.3:c.830A>T
MANE Select
|
NP_056477.1:p.Glu277Val
|
|
