ENST00000697149.1:c.1616G>A
|
ENSP00000513138.1:n.1616G>A
|
|
ENST00000697150.1:c.1674G>A
|
ENSP00000513139.1:n.1674G>A
|
|
ENST00000697151.1:c.1607G>A
|
ENSP00000513140.1:n.1607G>A
|
|
ENST00000697164.1:c.1687G>A
|
ENSP00000513153.1:p.Glu563Lys
|
|
ENST00000697165.1:c.1474G>A
|
ENSP00000513154.1:p.Glu492Lys
|
|
ENST00000347310.10:c.1777G>A
MANE Select
|
ENSP00000321345.5:p.Glu593Lys
|
|
ENST00000637002.1:c.1168G>A
|
ENSP00000490340.1:p.Glu390Lys
|
|
ENST00000347310.9:c.1777G>A
|
ENSP00000321345.5:p.Glu593Lys
|
|
ENST00000395227.2:c.571G>A
|
ENSP00000378652.2:p.Glu191Lys
|
|
ENST00000425614.3:c.1012G>A
|
ENSP00000387640.2:p.Glu338Lys
|
|
ENST00000473881.2:c.*603G>A
|
ENSP00000486667.1:n.*603G>A
|
|
NM_144701.2:c.1777G>A
|
NP_653302.2:p.Glu593Lys
|
|
XM_005270516.2:c.1015G>A
|
XP_005270573.1:p.Glu339Lys
|
|
XM_011540789.1:c.1867G>A
|
XP_011539091.1:p.Glu623Lys
|
|
XM_011540790.1:c.1777G>A
|
XP_011539092.1:p.Glu593Lys
|
|
XM_011540791.1:c.1777G>A
|
XP_011539093.1:p.Glu593Lys
|
|
XM_011540790.3:c.1777G>A
|
XP_011539092.1:p.Glu593Lys
|
|
XM_011540791.3:c.1777G>A
|
XP_011539093.1:p.Glu593Lys
|
|
XR_001736993.1:n.1857G>A
|
|
|
NM_144701.3:c.1777G>A
MANE Select
|
NP_653302.2:p.Glu593Lys
|
|