ENST00000697149.1:c.1722A>C
|
ENSP00000513138.1:n.1722A>C
|
|
ENST00000697150.1:c.1780A>C
|
ENSP00000513139.1:n.1780A>C
|
|
ENST00000697151.1:c.1713A>C
|
ENSP00000513140.1:n.1713A>C
|
|
ENST00000697164.1:c.1793A>C
|
ENSP00000513153.1:p.Glu598Ala
|
|
ENST00000697165.1:c.1580A>C
|
ENSP00000513154.1:p.Glu527Ala
|
|
ENST00000347310.10:c.1883A>C
MANE Select
|
ENSP00000321345.5:p.Glu628Ala
|
|
ENST00000637002.1:c.1274A>C
|
ENSP00000490340.1:p.Glu425Ala
|
|
ENST00000347310.9:c.1883A>C
|
ENSP00000321345.5:p.Glu628Ala
|
|
ENST00000395227.2:c.677A>C
|
ENSP00000378652.2:p.Glu226Ala
|
|
ENST00000425614.3:c.1118A>C
|
ENSP00000387640.2:p.Glu373Ala
|
|
ENST00000473881.2:c.*709A>C
|
ENSP00000486667.1:n.*709A>C
|
|
NM_144701.2:c.1883A>C
|
NP_653302.2:p.Glu628Ala
|
|
XM_005270516.2:c.1121A>C
|
XP_005270573.1:p.Glu374Ala
|
|
XM_011540789.1:c.1973A>C
|
XP_011539091.1:p.Glu658Ala
|
|
XM_011540790.1:c.1883A>C
|
XP_011539092.1:p.Glu628Ala
|
|
XM_011540791.1:c.1883A>C
|
XP_011539093.1:p.Glu628Ala
|
|
XM_011540790.3:c.1883A>C
|
XP_011539092.1:p.Glu628Ala
|
|
XM_011540791.3:c.1883A>C
|
XP_011539093.1:p.Glu628Ala
|
|
XR_001736993.1:n.1963A>C
|
|
|
NM_144701.3:c.1883A>C
MANE Select
|
NP_653302.2:p.Glu628Ala
|
|