ENST00000682617.1:c.2561C>A
|
ENSP00000507912.1:p.Ala854Glu
|
|
ENST00000683962.1:c.*2117C>A
|
ENSP00000506854.1:n.*2117C>A
|
|
ENST00000311895.8:c.2423C>A
MANE Select
|
ENSP00000310520.7:p.Ala808Glu
|
|
ENST00000311895.7:c.2423C>A
|
ENSP00000310520.7:p.Ala808Glu
|
|
ENST00000389138.7:n.1700C>A
|
|
|
NM_005236.2:c.2423C>A , LRG_463t1:c.2423C>A
|
NP_005227.1:p.Ala808Glu
|
|
XM_011522424.1:c.2561C>A
|
XP_011520726.1:p.Ala854Glu
|
|
XM_011522425.1:c.1880C>A
|
XP_011520727.1:p.Ala627Glu
|
|
XM_011522426.1:c.1634C>A
|
XP_011520728.1:p.Ala545Glu
|
|
XM_011522427.1:c.1073C>A
|
XP_011520729.1:p.Ala358Glu
|
|
XR_932805.1:n.2582C>A
|
|
|
XM_011522424.3:c.2561C>A
|
XP_011520726.1:p.Ala854Glu
|
|
XM_017023043.2:c.1634C>A
|
XP_016878532.1:p.Ala545Glu
|
|
NM_005236.3:c.2423C>A
MANE Select
|
NP_005227.1:p.Ala808Glu
|
|