|
NM_144701.3:c.1882G>A
MANE Select
|
NP_653302.2:p.Glu628Lys
|
|
ENST00000347310.10:c.1882G>A
MANE Select
|
ENSP00000321345.5:p.Glu628Lys
|
|
NM_144701.2:c.1882G>A
|
NP_653302.2:p.Glu628Lys
|
|
ENST00000347310.9:c.1882G>A
|
ENSP00000321345.5:p.Glu628Lys
|
|
ENST00000395227.2:c.676G>A
|
ENSP00000378652.2:p.Glu226Lys
|
|
ENST00000425614.3:c.1117G>A
|
ENSP00000387640.2:p.Glu373Lys
|
|
ENST00000473881.2:c.*708G>A
|
ENSP00000486667.1:n.*708G>A
|
|
ENST00000637002.1:c.1273G>A
|
ENSP00000490340.1:p.Glu425Lys
|
|
ENST00000697149.1:c.1721G>A
|
ENSP00000513138.1:n.1721G>A
|
|
ENST00000697150.1:c.1779G>A
|
ENSP00000513139.1:n.1779G>A
|
|
ENST00000697151.1:c.1712G>A
|
ENSP00000513140.1:n.1712G>A
|
|
ENST00000697164.1:c.1792G>A
|
ENSP00000513153.1:p.Glu598Lys
|
|
ENST00000697165.1:c.1579G>A
|
ENSP00000513154.1:p.Glu527Lys
|
|
XM_005270516.2:c.1120G>A
|
XP_005270573.1:p.Glu374Lys
|
|
XM_011540789.1:c.1972G>A
|
XP_011539091.1:p.Glu658Lys
|
|
XM_011540790.1:c.1882G>A
|
XP_011539092.1:p.Glu628Lys
|
|
XM_011540790.3:c.1882G>A
|
XP_011539092.1:p.Glu628Lys
|
|
XM_011540791.1:c.1882G>A
|
XP_011539093.1:p.Glu628Lys
|
|
XM_011540791.3:c.1882G>A
|
XP_011539093.1:p.Glu628Lys
|
|
XR_001736993.1:n.1962G>A
|
|