| NM_000795.4:c.939T>C
                    
                              MANE Select | NP_000786.1:p.His313= | 
            
              | ENST00000362072.8:c.939T>C
                    
                        MANE Select | ENSP00000354859.3:p.His313= | 
            
              | NM_000795.3:c.939T>C | NP_000786.1:p.His313= | 
            
              | NM_016574.3:c.852T>C | NP_057658.2:p.His284= | 
            
              | NM_016574.4:c.852T>C | NP_057658.2:p.His284= | 
            
              | ENST00000346454.7:c.852T>C | ENSP00000278597.5:p.His284= | 
            
              | ENST00000362072.7:c.939T>C | ENSP00000354859.3:p.His313= | 
            
              | ENST00000538967.5:c.945T>C | ENSP00000438215.1:p.His315= | 
            
              | ENST00000542968.5:c.939T>C | ENSP00000442172.1:p.His313= | 
            
              | ENST00000544518.5:c.936T>C | ENSP00000441068.1:p.His312= | 
            
              | XM_017017296.2:c.939T>C | XP_016872785.1:p.His313= |