| 
                  NM_000166.6:c.711C>T
                    
                              MANE Select
                      
               | 
              
                  
                    NP_000157.1:p.His237=
                  
               | 
            
            
              | 
                  ENST00000361726.7:c.711C>T
                    
                        MANE Select
                      
               | 
              
                  
                    ENSP00000354900.6:p.His237=
                  
               | 
            
            
              | 
                  NM_000166.5:c.711C>T
               | 
              
                  
                    NP_000157.1:p.His237=
                  
               | 
            
            
              | 
                  NM_001097642.2:c.711C>T , LRG_245t1:c.711C>T
               | 
              
                  
                    NP_001091111.1:p.His237=
                  
               | 
            
            
              | 
                  NM_001097642.3:c.711C>T
               | 
              
                  
                    NP_001091111.1:p.His237=
                  
               | 
            
            
              | 
                  ENST00000361726.6:c.711C>T
               | 
              
                  
                    ENSP00000354900.6:p.His237=
                  
               | 
            
            
              | 
                  ENST00000374022.3:c.711C>T
               | 
              
                  
                    ENSP00000363134.3:p.His237=
                  
               | 
            
            
              | 
                  ENST00000374029.1:c.711C>T
               | 
              
                  
                    ENSP00000363141.1:p.His237=
                  
               | 
            
            
              | 
                  ENST00000374029.2:c.711C>T
               | 
              
                  
                    ENSP00000363141.1:p.His237=
                  
               | 
            
            
              | 
                  ENST00000447581.2:c.711C>T
               | 
              
                  
                    ENSP00000407223.2:p.His237=
                  
               | 
            
            
              | 
                  ENST00000645009.2:c.711C>T
               | 
              
                  
                    ENSP00000494142.2:p.His237=
                  
               | 
            
            
              | 
                  ENST00000646835.1:c.711C>T
               | 
              
                  
                    ENSP00000494596.1:p.His237=
                  
               | 
            
            
              | 
                  ENST00000647424.1:c.711C>T
               | 
              
                  
                    ENSP00000495960.1:p.His237=
                  
               | 
            
            
              | 
                  ENST00000674549.1:c.711C>T
               | 
              
                  
                    ENSP00000502766.1:p.His237=
                  
               | 
            
            
              | 
                  ENST00000674844.1:c.711C>T
               | 
              
                  
                    ENSP00000502556.1:p.His237=
                  
               | 
            
            
              | 
                  ENST00000675209.1:c.711C>T
               | 
              
                  
                    ENSP00000501813.1:p.His237=
                  
               | 
            
            
              | 
                  ENST00000675368.1:c.711C>T
               | 
              
                  
                    ENSP00000501757.1:p.His237=
                  
               | 
            
            
              | 
                  ENST00000675609.1:c.711C>T
               | 
              
                  
                    ENSP00000501571.1:p.His237=
                  
               | 
            
            
              | 
                  XM_011530907.1:c.711C>T
               | 
              
                  
                    XP_011529209.1:p.His237=
                  
               | 
            
            
              | 
                  XM_011530907.2:c.711C>T
               | 
              
                  
                    XP_011529209.1:p.His237=
                  
               |