ENST00000697149.1:c.1693A>C
|
ENSP00000513138.1:n.1693A>C
|
|
ENST00000697150.1:c.1751A>C
|
ENSP00000513139.1:n.1751A>C
|
|
ENST00000697151.1:c.1684A>C
|
ENSP00000513140.1:n.1684A>C
|
|
ENST00000697164.1:c.1764A>C
|
ENSP00000513153.1:p.Glu588Asp
|
|
ENST00000697165.1:c.1551A>C
|
ENSP00000513154.1:p.Glu517Asp
|
|
ENST00000347310.10:c.1854A>C
MANE Select
|
ENSP00000321345.5:p.Glu618Asp
|
|
ENST00000637002.1:c.1245A>C
|
ENSP00000490340.1:p.Glu415Asp
|
|
ENST00000347310.9:c.1854A>C
|
ENSP00000321345.5:p.Glu618Asp
|
|
ENST00000395227.2:c.648A>C
|
ENSP00000378652.2:p.Glu216Asp
|
|
ENST00000425614.3:c.1089A>C
|
ENSP00000387640.2:p.Glu363Asp
|
|
ENST00000473881.2:c.*680A>C
|
ENSP00000486667.1:n.*680A>C
|
|
NM_144701.2:c.1854A>C
|
NP_653302.2:p.Glu618Asp
|
|
XM_005270516.2:c.1092A>C
|
XP_005270573.1:p.Glu364Asp
|
|
XM_011540789.1:c.1944A>C
|
XP_011539091.1:p.Glu648Asp
|
|
XM_011540790.1:c.1854A>C
|
XP_011539092.1:p.Glu618Asp
|
|
XM_011540791.1:c.1854A>C
|
XP_011539093.1:p.Glu618Asp
|
|
XM_011540790.3:c.1854A>C
|
XP_011539092.1:p.Glu618Asp
|
|
XM_011540791.3:c.1854A>C
|
XP_011539093.1:p.Glu618Asp
|
|
XR_001736993.1:n.1934A>C
|
|
|
NM_144701.3:c.1854A>C
MANE Select
|
NP_653302.2:p.Glu618Asp
|
|