| 
                  NM_017774.3:c.371+38513T>G
                    
                              MANE Select
                      
               | 
              
                  
                    NP_060244.2:n.371+38513T>G
                  
               | 
            
            
              | 
                  ENST00000274695.8:c.371+38513T>G
                    
                        MANE Select
                      
               | 
              
                  
                    ENSP00000274695.4:n.371+38513T>G
                  
               | 
            
            
              | 
                  ENST00000378610.1:c.371+38513T>G
               | 
              
                  
                    ENSP00000367873.1:n.371+38513T>G
                  
               | 
            
            
              | 
                  XM_006715128.2:c.371+38513T>G
               | 
              
                  
                    XP_006715191.1:n.371+38513T>G
                  
               | 
            
            
              | 
                  XM_011514718.1:c.371+38513T>G
               | 
              
                  
                    XP_011513020.1:n.371+38513T>G
                  
               | 
            
            
              | 
                  XM_011514719.1:c.371+38513T>G
               | 
              
                  
                    XP_011513021.1:n.371+38513T>G
                  
               | 
            
            
              | 
                  XM_011514719.2:c.371+38513T>G
               | 
              
                  
                    XP_011513021.1:n.371+38513T>G
                  
               | 
            
            
              | 
                  XM_017010986.1:c.371+38513T>G
               | 
              
                  
                    XP_016866475.1:n.371+38513T>G
                  
               | 
            
            
              | 
                  XM_017010987.1:c.-384+38513T>G
               | 
              
                  
                    XP_016866476.1:n.-384+38513T>G
                  
               | 
            
            
              | 
                  XM_024446481.1:c.371+38513T>G
               | 
              
                  
                    XP_024302249.1:n.371+38513T>G
                  
               | 
            
            
              | 
                  XR_001743495.2:n.543+38513T>G
               | 
              
                  
               | 
            
            
              | 
                  XR_001743496.2:n.938+38513T>G
               | 
              
                  
               | 
            
            
              | 
                  XR_001743500.1:n.538+38513T>G
               | 
              
                  
               | 
            
            
              | 
                  XR_001743501.1:n.538+38513T>G
               | 
              
                  
               | 
            
            
              | 
                  XR_926265.1:n.538+38513T>G
               | 
              
                  
               | 
            
            
              | 
                  XR_926265.2:n.538+38513T>G
               | 
              
                  
               | 
            
            
              | 
                  XR_926266.1:n.651+38513T>G
               | 
              
                  
               | 
            
            
              | 
                  XR_926266.2:n.651+38513T>G
               | 
              
                  
               | 
            
            
              | 
                  XR_926267.1:n.538+38513T>G
               | 
              
                  
               | 
            
            
              | 
                  XR_926267.2:n.538+38513T>G
               | 
              
                  
               |