ENST00000697149.1:c.1436T>A
|
ENSP00000513138.1:n.1436T>A
|
|
ENST00000697150.1:c.1494T>A
|
ENSP00000513139.1:n.1494T>A
|
|
ENST00000697151.1:c.1427T>A
|
ENSP00000513140.1:n.1427T>A
|
|
ENST00000697164.1:c.1507T>A
|
ENSP00000513153.1:p.Ser503Thr
|
|
ENST00000697165.1:c.1294T>A
|
ENSP00000513154.1:p.Ser432Thr
|
|
ENST00000347310.10:c.1597T>A
MANE Select
|
ENSP00000321345.5:p.Ser533Thr
|
|
ENST00000637002.1:c.988T>A
|
ENSP00000490340.1:p.Ser330Thr
|
|
ENST00000347310.9:c.1597T>A
|
ENSP00000321345.5:p.Ser533Thr
|
|
ENST00000395227.2:c.391T>A
|
ENSP00000378652.2:p.Ser131Thr
|
|
ENST00000425614.3:c.832T>A
|
ENSP00000387640.2:p.Ser278Thr
|
|
ENST00000473881.2:c.*423T>A
|
ENSP00000486667.1:n.*423T>A
|
|
NM_144701.2:c.1597T>A
|
NP_653302.2:p.Ser533Thr
|
|
XM_005270516.2:c.835T>A
|
XP_005270573.1:p.Ser279Thr
|
|
XM_011540789.1:c.1687T>A
|
XP_011539091.1:p.Ser563Thr
|
|
XM_011540790.1:c.1597T>A
|
XP_011539092.1:p.Ser533Thr
|
|
XM_011540791.1:c.1597T>A
|
XP_011539093.1:p.Ser533Thr
|
|
XM_011540790.3:c.1597T>A
|
XP_011539092.1:p.Ser533Thr
|
|
XM_011540791.3:c.1597T>A
|
XP_011539093.1:p.Ser533Thr
|
|
XR_001736993.1:n.1677T>A
|
|
|
NM_144701.3:c.1597T>A
MANE Select
|
NP_653302.2:p.Ser533Thr
|
|