| NM_054012.4:c.847G=
                    
                              MANE Select | NP_446464.1:p.Glu283= | 
            
              | ENST00000352480.10:c.847G=
                    
                        MANE Select | ENSP00000253004.6:p.Glu283= | 
            
              | NM_000050.4:c.847G= | NP_000041.2:p.Glu283= | 
            
              | NM_054012.3:c.847G= | NP_446464.1:p.Glu283= | 
            
              | ENST00000352480.9:c.847G= | ENSP00000253004.6:p.Glu283= | 
            
              | ENST00000372386.6:n.118G= |  | 
            
              | ENST00000372393.7:c.847G= | ENSP00000361469.2:p.Glu283= | 
            
              | ENST00000372394.5:c.847G= | ENSP00000361471.1:p.Glu283= | 
            
              | ENST00000470849.4:n.572G= |  | 
            
              | ENST00000492400.5:n.356G= |  | 
            
              | ENST00000493984.6:n.624G= |  | 
            
              | XM_005272200.2:c.847G= | XP_005272257.1:p.Glu283= | 
            
              | XM_005272200.3:c.847G= | XP_005272257.1:p.Glu283= | 
            
              | XM_011518705.1:c.961G= | XP_011517007.1:p.Glu321= | 
            
              | XM_011518705.2:c.961G= | XP_011517007.1:p.Glu321= | 
            
              | XM_017014729.1:c.943G= | XP_016870218.1:p.Glu315= |