| NM_033100.4:c.2197G>T
                    
                              MANE Select | NP_149091.1:p.Val733Phe | 
            
              | ENST00000623527.4:c.2197G>T
                    
                        MANE Select | ENSP00000485478.1:p.Val733Phe | 
            
              | NM_001171971.2:c.2040+890G>T | NP_001165442.1:n.2040+890G>T | 
            
              | NM_001171971.3:c.2040+890G>T | NP_001165442.1:n.2040+890G>T | 
            
              | NM_033100.3:c.2197G>T | NP_149091.1:p.Val733Phe | 
            
              | ENST00000332904.7:c.2040+890G>T | ENSP00000331063.3:n.2040+890G>T | 
            
              | ENST00000372117.6:c.1412G>T |  | 
            
              | ENST00000459673.1:n.629G>T |  | 
            
              | ENST00000623399.1:c.211+890G>T |  | 
            
              | ENST00000623527.3:c.2197G>T | ENSP00000485478.1:p.Val733Phe | 
            
              | XM_011540337.1:c.2371G>T | XP_011538639.1:p.Val791Phe | 
            
              | XM_011540338.1:c.2214+890G>T | XP_011538640.1:n.2214+890G>T | 
            
              | XM_011540339.1:c.1750G>T | XP_011538641.1:p.Val584Phe |