ENST00000697149.1:c.1573T>C
|
ENSP00000513138.1:n.1573T>C
|
|
ENST00000697150.1:c.1631T>C
|
ENSP00000513139.1:n.1631T>C
|
|
ENST00000697151.1:c.1564T>C
|
ENSP00000513140.1:n.1564T>C
|
|
ENST00000697164.1:c.1644T>C
|
ENSP00000513153.1:p.Asp548=
|
|
ENST00000697165.1:c.1431T>C
|
ENSP00000513154.1:p.Asp477=
|
|
ENST00000347310.10:c.1734T>C
MANE Select
|
ENSP00000321345.5:p.Asp578=
|
|
ENST00000637002.1:c.1125T>C
|
ENSP00000490340.1:p.Asp375=
|
|
ENST00000347310.9:c.1734T>C
|
ENSP00000321345.5:p.Asp578=
|
|
ENST00000395227.2:c.528T>C
|
ENSP00000378652.2:p.Asp176=
|
|
ENST00000425614.3:c.969T>C
|
ENSP00000387640.2:p.Asp323=
|
|
ENST00000473881.2:c.*560T>C
|
ENSP00000486667.1:n.*560T>C
|
|
NM_144701.2:c.1734T>C
|
NP_653302.2:p.Asp578=
|
|
XM_005270516.2:c.972T>C
|
XP_005270573.1:p.Asp324=
|
|
XM_011540789.1:c.1824T>C
|
XP_011539091.1:p.Asp608=
|
|
XM_011540790.1:c.1734T>C
|
XP_011539092.1:p.Asp578=
|
|
XM_011540791.1:c.1734T>C
|
XP_011539093.1:p.Asp578=
|
|
XM_011540790.3:c.1734T>C
|
XP_011539092.1:p.Asp578=
|
|
XM_011540791.3:c.1734T>C
|
XP_011539093.1:p.Asp578=
|
|
XR_001736993.1:n.1814T>C
|
|
|
NM_144701.3:c.1734T>C
MANE Select
|
NP_653302.2:p.Asp578=
|
|