ENST00000697149.1:c.1648G>T
|
ENSP00000513138.1:n.1648G>T
|
|
ENST00000697150.1:c.1706G>T
|
ENSP00000513139.1:n.1706G>T
|
|
ENST00000697151.1:c.1639G>T
|
ENSP00000513140.1:n.1639G>T
|
|
ENST00000697164.1:c.1719G>T
|
ENSP00000513153.1:p.Glu573Asp
|
|
ENST00000697165.1:c.1506G>T
|
ENSP00000513154.1:p.Glu502Asp
|
|
ENST00000347310.10:c.1809G>T
MANE Select
|
ENSP00000321345.5:p.Glu603Asp
|
|
ENST00000637002.1:c.1200G>T
|
ENSP00000490340.1:p.Glu400Asp
|
|
ENST00000347310.9:c.1809G>T
|
ENSP00000321345.5:p.Glu603Asp
|
|
ENST00000395227.2:c.603G>T
|
ENSP00000378652.2:p.Glu201Asp
|
|
ENST00000425614.3:c.1044G>T
|
ENSP00000387640.2:p.Glu348Asp
|
|
ENST00000473881.2:c.*635G>T
|
ENSP00000486667.1:n.*635G>T
|
|
NM_144701.2:c.1809G>T
|
NP_653302.2:p.Glu603Asp
|
|
XM_005270516.2:c.1047G>T
|
XP_005270573.1:p.Glu349Asp
|
|
XM_011540789.1:c.1899G>T
|
XP_011539091.1:p.Glu633Asp
|
|
XM_011540790.1:c.1809G>T
|
XP_011539092.1:p.Glu603Asp
|
|
XM_011540791.1:c.1809G>T
|
XP_011539093.1:p.Glu603Asp
|
|
XM_011540790.3:c.1809G>T
|
XP_011539092.1:p.Glu603Asp
|
|
XM_011540791.3:c.1809G>T
|
XP_011539093.1:p.Glu603Asp
|
|
XR_001736993.1:n.1889G>T
|
|
|
NM_144701.3:c.1809G>T
MANE Select
|
NP_653302.2:p.Glu603Asp
|
|