| 
                  NM_005458.8:c.1893+1661A>G
                    
                              MANE Select
                      
               | 
              
                  
                    NP_005449.5:n.1893+1661A>G
                  
               | 
            
            
              | 
                  ENST00000259455.4:c.1893+1661A>G
                    
                        MANE Select
                      
               | 
              
                  
                    ENSP00000259455.2:n.1893+1661A>G
                  
               | 
            
            
              | 
                  NM_005458.7:c.1893+1661A>G
               | 
              
                  
                    NP_005449.5:n.1893+1661A>G
                  
               | 
            
            
              | 
                  ENST00000259455.3:c.1893+1661A>G
               | 
              
                  
                    ENSP00000259455.2:n.1893+1661A>G
                  
               | 
            
            
              | 
                  ENST00000634457.1:c.231+1661A>G
               | 
              
                  
                    ENSP00000489352.1:n.231+1661A>G
                  
               | 
            
            
              | 
                  ENST00000635462.1:n.388+1661A>G
               | 
              
                  
               | 
            
            
              | 
                  ENST00000637410.1:n.1671+1661A>G
               | 
              
                  
               | 
            
            
              | 
                  XM_005252316.3:c.1119+1661A>G
               | 
              
                  
                    XP_005252373.1:n.1119+1661A>G
                  
               | 
            
            
              | 
                  XM_005252316.5:c.1119+1661A>G
               | 
              
                  
                    XP_005252373.1:n.1119+1661A>G
                  
               | 
            
            
              | 
                  XM_017015331.2:c.1599+1661A>G
               | 
              
                  
                    XP_016870820.1:n.1599+1661A>G
                  
               | 
            
            
              | 
                  XM_017015332.2:c.1119+1661A>G
               | 
              
                  
                    XP_016870821.1:n.1119+1661A>G
                  
               |