| NM_144701.3:c.*337C>T
                    
                              MANE Select | NP_653302.2:n.*337C>T | 
            
              | ENST00000347310.10:c.*337C>T
                    
                        MANE Select | ENSP00000321345.5:n.*337C>T | 
            
              | NM_144701.2:c.*337C>T | NP_653302.2:n.*337C>T | 
            
              | ENST00000347310.9:c.*337C>T | ENSP00000321345.5:n.*337C>T | 
            
              | ENST00000395227.2:c.*337C>T | ENSP00000378652.2:n.*337C>T | 
            
              | ENST00000473881.2:c.*1053C>T | ENSP00000486667.1:n.*1053C>T | 
            
              | XM_005270516.2:c.*337C>T | XP_005270573.1:n.*337C>T | 
            
              | XM_011540789.1:c.*337C>T | XP_011539091.1:n.*337C>T | 
            
              | XM_011540790.1:c.*337C>T | XP_011539092.1:n.*337C>T | 
            
              | XM_011540790.3:c.*337C>T | XP_011539092.1:n.*337C>T | 
            
              | XM_011540791.1:c.*337C>T | XP_011539093.1:n.*337C>T | 
            
              | XM_011540791.3:c.*337C>T | XP_011539093.1:n.*337C>T |