| NM_033100.4:c.1219C>T
                    
                              MANE Select | NP_149091.1:p.Arg407Ter | 
            
              | ENST00000623527.4:c.1219C>T
                    
                        MANE Select | ENSP00000485478.1:p.Arg407Ter | 
            
              | NM_001171971.2:c.1219C>T | NP_001165442.1:p.Arg407Ter | 
            
              | NM_001171971.3:c.1219C>T | NP_001165442.1:p.Arg407Ter | 
            
              | NM_033100.3:c.1219C>T | NP_149091.1:p.Arg407Ter | 
            
              | ENST00000332904.7:c.1219C>T | ENSP00000331063.3:p.Arg407Ter | 
            
              | ENST00000372117.6:c.599C>T |  | 
            
              | ENST00000623527.3:c.1219C>T | ENSP00000485478.1:p.Arg407Ter | 
            
              | ENST00000624091.1:c.505C>T |  | 
            
              | XM_011540337.1:c.1393C>T | XP_011538639.1:p.Arg465Ter | 
            
              | XM_011540338.1:c.1393C>T | XP_011538640.1:p.Arg465Ter | 
            
              | XM_011540339.1:c.772C>T | XP_011538641.1:p.Arg258Ter | 
            
              | XM_011540340.1:c.1393C>T | XP_011538642.1:p.Arg465Ter | 
            
              | XM_011540340.3:c.1393C>T | XP_011538642.1:p.Arg465Ter |