| NM_000660.7:c.652C=
                    
                              MANE Select | NP_000651.3:p.Arg218= | 
            
              | ENST00000221930.6:c.652C=
                    
                        MANE Select | ENSP00000221930.4:p.Arg218= | 
            
              | NM_000660.5:c.652C= | NP_000651.3:p.Arg218= | 
            
              | NM_000660.6:c.652C= | NP_000651.3:p.Arg218= | 
            
              | ENST00000221930.5:c.652C= | ENSP00000221930.4:p.Arg218= | 
            
              | ENST00000597453.1:n.183C= |  | 
            
              | ENST00000600196.1:n.112C= |  | 
            
              | ENST00000600196.2:c.652C= | ENSP00000504008.1:p.Arg218= | 
            
              | ENST00000677934.1:c.634+2517C= | ENSP00000504769.1:n.634+2517C= | 
            
              | XM_011527242.1:c.652C= | XP_011525544.1:p.Arg218= | 
            
              | XM_011527242.2:c.652C= | XP_011525544.1:p.Arg218= |