ENST00000697149.1:c.1506G>A
|
ENSP00000513138.1:n.1506G>A
|
|
ENST00000697150.1:c.1564G>A
|
ENSP00000513139.1:n.1564G>A
|
|
ENST00000697151.1:c.1497G>A
|
ENSP00000513140.1:n.1497G>A
|
|
ENST00000697164.1:c.1577G>A
|
ENSP00000513153.1:p.Gly526Glu
|
|
ENST00000697165.1:c.1364G>A
|
ENSP00000513154.1:p.Gly455Glu
|
|
ENST00000347310.10:c.1667G>A
MANE Select
|
ENSP00000321345.5:p.Gly556Glu
|
|
ENST00000637002.1:c.1058G>A
|
ENSP00000490340.1:p.Gly353Glu
|
|
ENST00000347310.9:c.1667G>A
|
ENSP00000321345.5:p.Gly556Glu
|
|
ENST00000395227.2:c.461G>A
|
ENSP00000378652.2:p.Gly154Glu
|
|
ENST00000425614.3:c.902G>A
|
ENSP00000387640.2:p.Gly301Glu
|
|
ENST00000473881.2:c.*493G>A
|
ENSP00000486667.1:n.*493G>A
|
|
NM_144701.2:c.1667G>A
|
NP_653302.2:p.Gly556Glu
|
|
XM_005270516.2:c.905G>A
|
XP_005270573.1:p.Gly302Glu
|
|
XM_011540789.1:c.1757G>A
|
XP_011539091.1:p.Gly586Glu
|
|
XM_011540790.1:c.1667G>A
|
XP_011539092.1:p.Gly556Glu
|
|
XM_011540791.1:c.1667G>A
|
XP_011539093.1:p.Gly556Glu
|
|
XM_011540790.3:c.1667G>A
|
XP_011539092.1:p.Gly556Glu
|
|
XM_011540791.3:c.1667G>A
|
XP_011539093.1:p.Gly556Glu
|
|
XR_001736993.1:n.1747G>A
|
|
|
NM_144701.3:c.1667G>A
MANE Select
|
NP_653302.2:p.Gly556Glu
|
|