ENST00000697149.1:c.1597A>G
|
ENSP00000513138.1:n.1597A>G
|
|
ENST00000697150.1:c.1655A>G
|
ENSP00000513139.1:n.1655A>G
|
|
ENST00000697151.1:c.1588A>G
|
ENSP00000513140.1:n.1588A>G
|
|
ENST00000697164.1:c.1668A>G
|
ENSP00000513153.1:p.Glu556=
|
|
ENST00000697165.1:c.1455A>G
|
ENSP00000513154.1:p.Glu485=
|
|
ENST00000347310.10:c.1758A>G
MANE Select
|
ENSP00000321345.5:p.Glu586=
|
|
ENST00000637002.1:c.1149A>G
|
ENSP00000490340.1:p.Glu383=
|
|
ENST00000347310.9:c.1758A>G
|
ENSP00000321345.5:p.Glu586=
|
|
ENST00000395227.2:c.552A>G
|
ENSP00000378652.2:p.Glu184=
|
|
ENST00000425614.3:c.993A>G
|
ENSP00000387640.2:p.Glu331=
|
|
ENST00000473881.2:c.*584A>G
|
ENSP00000486667.1:n.*584A>G
|
|
NM_144701.2:c.1758A>G
|
NP_653302.2:p.Glu586=
|
|
XM_005270516.2:c.996A>G
|
XP_005270573.1:p.Glu332=
|
|
XM_011540789.1:c.1848A>G
|
XP_011539091.1:p.Glu616=
|
|
XM_011540790.1:c.1758A>G
|
XP_011539092.1:p.Glu586=
|
|
XM_011540791.1:c.1758A>G
|
XP_011539093.1:p.Glu586=
|
|
XM_011540790.3:c.1758A>G
|
XP_011539092.1:p.Glu586=
|
|
XM_011540791.3:c.1758A>G
|
XP_011539093.1:p.Glu586=
|
|
XR_001736993.1:n.1838A>G
|
|
|
NM_144701.3:c.1758A>G
MANE Select
|
NP_653302.2:p.Glu586=
|
|