| NM_144701.3:c.*212T>C
                    
                              MANE Select | NP_653302.2:n.*212T>C | 
            
              | ENST00000347310.10:c.*212T>C
                    
                        MANE Select | ENSP00000321345.5:n.*212T>C | 
            
              | NM_144701.2:c.*212T>C | NP_653302.2:n.*212T>C | 
            
              | ENST00000347310.9:c.*212T>C | ENSP00000321345.5:n.*212T>C | 
            
              | ENST00000395227.2:c.*212T>C | ENSP00000378652.2:n.*212T>C | 
            
              | ENST00000473881.2:c.*928T>C | ENSP00000486667.1:n.*928T>C | 
            
              | XM_005270516.2:c.*212T>C | XP_005270573.1:n.*212T>C | 
            
              | XM_011540789.1:c.*212T>C | XP_011539091.1:n.*212T>C | 
            
              | XM_011540790.1:c.*212T>C | XP_011539092.1:n.*212T>C | 
            
              | XM_011540790.3:c.*212T>C | XP_011539092.1:n.*212T>C | 
            
              | XM_011540791.1:c.*212T>C | XP_011539093.1:n.*212T>C | 
            
              | XM_011540791.3:c.*212T>C | XP_011539093.1:n.*212T>C |