| NM_033100.4:c.*2577G>C
                    
                              MANE Select | NP_149091.1:n.*2577G>C | 
            
              | ENST00000623527.4:c.*2577G>C
                    
                        MANE Select | ENSP00000485478.1:n.*2577G>C | 
            
              | NM_001171971.2:c.2041-1881G>C | NP_001165442.1:n.2041-1881G>C | 
            
              | NM_001171971.3:c.2041-1881G>C | NP_001165442.1:n.2041-1881G>C | 
            
              | NM_033100.3:c.*2577G>C | NP_149091.1:n.*2577G>C | 
            
              | ENST00000332904.7:c.2041-1881G>C | ENSP00000331063.3:n.2041-1881G>C | 
            
              | ENST00000372117.6:c.4372G>C |  | 
            
              | ENST00000459673.1:n.3589G>C |  | 
            
              | ENST00000623399.1:c.212-1881G>C |  | 
            
              | ENST00000623527.3:c.*2577G>C | ENSP00000485478.1:n.*2577G>C | 
            
              | XM_011540337.1:c.*2577G>C | XP_011538639.1:n.*2577G>C | 
            
              | XM_011540338.1:c.2215-1881G>C | XP_011538640.1:n.2215-1881G>C | 
            
              | XM_011540339.1:c.*2577G>C | XP_011538641.1:n.*2577G>C |