| NM_173653.4:c.533+9310C>T
                    
                              MANE Select | NP_775924.1:n.533+9310C>T | 
            
              | ENST00000316549.11:c.533+9310C>T
                    
                        MANE Select | ENSP00000320246.6:n.533+9310C>T | 
            
              | NM_173653.3:c.533+9310C>T | NP_775924.1:n.533+9310C>T | 
            
              | ENST00000316549.10:c.533+9310C>T | ENSP00000320246.6:n.533+9310C>T | 
            
              | ENST00000474727.2:c.*144+9310C>T | ENSP00000419090.2:n.*144+9310C>T | 
            
              | XM_011512704.1:c.533+9310C>T | XP_011511006.1:n.533+9310C>T | 
            
              | XM_011512704.3:c.533+9310C>T | XP_011511006.1:n.533+9310C>T | 
            
              | XM_017006202.2:c.533+9310C>T | XP_016861691.1:n.533+9310C>T | 
            
              | XM_017006203.1:c.182+9310C>T | XP_016861692.1:n.182+9310C>T |