ENST00000697149.1:c.1549A>T
|
ENSP00000513138.1:n.1549A>T
|
|
ENST00000697150.1:c.1607A>T
|
ENSP00000513139.1:n.1607A>T
|
|
ENST00000697151.1:c.1540A>T
|
ENSP00000513140.1:n.1540A>T
|
|
ENST00000697164.1:c.1620A>T
|
ENSP00000513153.1:p.Glu540Asp
|
|
ENST00000697165.1:c.1407A>T
|
ENSP00000513154.1:p.Glu469Asp
|
|
ENST00000347310.10:c.1710A>T
MANE Select
|
ENSP00000321345.5:p.Glu570Asp
|
|
ENST00000637002.1:c.1101A>T
|
ENSP00000490340.1:p.Glu367Asp
|
|
ENST00000347310.9:c.1710A>T
|
ENSP00000321345.5:p.Glu570Asp
|
|
ENST00000395227.2:c.504A>T
|
ENSP00000378652.2:p.Glu168Asp
|
|
ENST00000425614.3:c.945A>T
|
ENSP00000387640.2:p.Glu315Asp
|
|
ENST00000473881.2:c.*536A>T
|
ENSP00000486667.1:n.*536A>T
|
|
NM_144701.2:c.1710A>T
|
NP_653302.2:p.Glu570Asp
|
|
XM_005270516.2:c.948A>T
|
XP_005270573.1:p.Glu316Asp
|
|
XM_011540789.1:c.1800A>T
|
XP_011539091.1:p.Glu600Asp
|
|
XM_011540790.1:c.1710A>T
|
XP_011539092.1:p.Glu570Asp
|
|
XM_011540791.1:c.1710A>T
|
XP_011539093.1:p.Glu570Asp
|
|
XM_011540790.3:c.1710A>T
|
XP_011539092.1:p.Glu570Asp
|
|
XM_011540791.3:c.1710A>T
|
XP_011539093.1:p.Glu570Asp
|
|
XR_001736993.1:n.1790A>T
|
|
|
NM_144701.3:c.1710A>T
MANE Select
|
NP_653302.2:p.Glu570Asp
|
|