ENST00000697149.1:c.1646G>A
|
ENSP00000513138.1:n.1646G>A
|
|
ENST00000697150.1:c.1704G>A
|
ENSP00000513139.1:n.1704G>A
|
|
ENST00000697151.1:c.1637G>A
|
ENSP00000513140.1:n.1637G>A
|
|
ENST00000697164.1:c.1717G>A
|
ENSP00000513153.1:p.Glu573Lys
|
|
ENST00000697165.1:c.1504G>A
|
ENSP00000513154.1:p.Glu502Lys
|
|
ENST00000347310.10:c.1807G>A
MANE Select
|
ENSP00000321345.5:p.Glu603Lys
|
|
ENST00000637002.1:c.1198G>A
|
ENSP00000490340.1:p.Glu400Lys
|
|
ENST00000347310.9:c.1807G>A
|
ENSP00000321345.5:p.Glu603Lys
|
|
ENST00000395227.2:c.601G>A
|
ENSP00000378652.2:p.Glu201Lys
|
|
ENST00000425614.3:c.1042G>A
|
ENSP00000387640.2:p.Glu348Lys
|
|
ENST00000473881.2:c.*633G>A
|
ENSP00000486667.1:n.*633G>A
|
|
NM_144701.2:c.1807G>A
|
NP_653302.2:p.Glu603Lys
|
|
XM_005270516.2:c.1045G>A
|
XP_005270573.1:p.Glu349Lys
|
|
XM_011540789.1:c.1897G>A
|
XP_011539091.1:p.Glu633Lys
|
|
XM_011540790.1:c.1807G>A
|
XP_011539092.1:p.Glu603Lys
|
|
XM_011540791.1:c.1807G>A
|
XP_011539093.1:p.Glu603Lys
|
|
XM_011540790.3:c.1807G>A
|
XP_011539092.1:p.Glu603Lys
|
|
XM_011540791.3:c.1807G>A
|
XP_011539093.1:p.Glu603Lys
|
|
XR_001736993.1:n.1887G>A
|
|
|
NM_144701.3:c.1807G>A
MANE Select
|
NP_653302.2:p.Glu603Lys
|
|