| NM_018490.5:c.286A>G
                    
                              MANE Select | NP_060960.2:p.Ile96Val | 
            
              | ENST00000379214.9:c.286A>G
                    
                        MANE Select | ENSP00000368516.4:p.Ile96Val | 
            
              | NM_001346432.1:c.214A>G | NP_001333361.1:p.Ile72Val | 
            
              | NM_001346432.2:c.214A>G | NP_001333361.1:p.Ile72Val | 
            
              | NM_018490.2:c.286A>G | NP_060960.2:p.Ile96Val | 
            
              | NM_018490.3:c.286A>G | NP_060960.2:p.Ile96Val | 
            
              | NM_018490.4:c.286A>G | NP_060960.2:p.Ile96Val | 
            
              | ENST00000379214.8:c.286A>G | ENSP00000368516.4:p.Ile96Val | 
            
              | ENST00000389858.4:c.214A>G | ENSP00000374508.4:p.Ile72Val | 
            
              | ENST00000480977.2:c.258-7022A>G | ENSP00000431650.1:n.258-7022A>G |