| 
                  NM_006129.5:c.2437G>A
                    
                              MANE Select
                      
               | 
              
                  
                    NP_006120.1:p.Ala813Thr
                      
                  
               | 
            
            
              | 
                  ENST00000306385.10:c.2437G>A
                    
                        MANE Select
                      
               | 
              
                  
                    ENSP00000305714.5:p.Ala813Thr
                      
                  
               | 
            
            
              | 
                  NM_006129.4:c.2437G>A
               | 
              
                  
                    NP_006120.1:p.Ala813Thr
                      
                  
               | 
            
            
              | 
                  NR_033403.1:n.2740G>A
               | 
              
                  
               | 
            
            
              | 
                  NR_033403.2:n.2508G>A
               | 
              
                  
               | 
            
            
              | 
                  ENST00000306385.9:c.2437G>A
               | 
              
                  
                    ENSP00000305714.5:p.Ala813Thr
                      
                  
               | 
            
            
              | 
                  ENST00000354870.5:c.*1694G>A
               | 
              
                  
                    ENSP00000346941.5:n.*1694G>A
                  
               | 
            
            
              | 
                  ENST00000520626.5:c.*2969G>A
               | 
              
                  
                    ENSP00000430015.1:n.*2969G>A
                  
               | 
            
            
              | 
                  ENST00000520626.6:c.*2969G>A
               | 
              
                  
                    ENSP00000430015.2:n.*2969G>A
                  
               | 
            
            
              | 
                  ENST00000520970.5:c.*801G>A
               | 
              
                  
                    ENSP00000428332.1:n.*801G>A
                  
               | 
            
            
              | 
                  ENST00000520982.5:c.*1904G>A
               | 
              
                  
                    ENSP00000428798.1:n.*1904G>A
                  
               | 
            
            
              | 
                  XR_001745579.2:n.3330G>A
               | 
              
                  
               | 
            
            
              | 
                  XR_949458.1:n.2810G>A
               | 
              
                  
               | 
            
            
              | 
                  XR_949458.2:n.2752G>A
               | 
              
                  
               |