ENST00000697149.1:c.1618A=
|
ENSP00000513138.1:n.1618A=
|
|
ENST00000697150.1:c.1676A=
|
ENSP00000513139.1:n.1676A=
|
|
ENST00000697151.1:c.1609A=
|
ENSP00000513140.1:n.1609A=
|
|
ENST00000697164.1:c.1689A=
|
ENSP00000513153.1:p.Glu563=
|
|
ENST00000697165.1:c.1476A=
|
ENSP00000513154.1:p.Glu492=
|
|
ENST00000347310.10:c.1779A=
MANE Select
|
ENSP00000321345.5:p.Glu593=
|
|
ENST00000637002.1:c.1170A=
|
ENSP00000490340.1:p.Glu390=
|
|
ENST00000347310.9:c.1779A=
|
ENSP00000321345.5:p.Glu593=
|
|
ENST00000395227.2:c.573A=
|
ENSP00000378652.2:p.Glu191=
|
|
ENST00000425614.3:c.1014A=
|
ENSP00000387640.2:p.Glu338=
|
|
ENST00000473881.2:c.*605A=
|
ENSP00000486667.1:n.*605A=
|
|
NM_144701.2:c.1779A=
|
NP_653302.2:p.Glu593=
|
|
XM_005270516.2:c.1017A=
|
XP_005270573.1:p.Glu339=
|
|
XM_011540789.1:c.1869A=
|
XP_011539091.1:p.Glu623=
|
|
XM_011540790.1:c.1779A=
|
XP_011539092.1:p.Glu593=
|
|
XM_011540791.1:c.1779A=
|
XP_011539093.1:p.Glu593=
|
|
XM_011540790.3:c.1779A=
|
XP_011539092.1:p.Glu593=
|
|
XM_011540791.3:c.1779A=
|
XP_011539093.1:p.Glu593=
|
|
XR_001736993.1:n.1859A=
|
|
|
NM_144701.3:c.1779A=
MANE Select
|
NP_653302.2:p.Glu593=
|
|