| NM_001002295.2:c.829C>A
                    
                              MANE Select | NP_001002295.1:p.Arg277= | 
            
              | ENST00000379328.9:c.829C>A
                    
                        MANE Select | ENSP00000368632.3:p.Arg277= | 
            
              | NM_001002295.1:c.829C>A | NP_001002295.1:p.Arg277= | 
            
              | NM_002051.2:c.826C>A | NP_002042.1:p.Arg276= | 
            
              | NM_002051.3:c.826C>A | NP_002042.1:p.Arg276= | 
            
              | ENST00000346208.3:c.826C>A | ENSP00000341619.3:p.Arg276= | 
            
              | ENST00000346208.4:c.826C>A | ENSP00000341619.3:p.Arg276= | 
            
              | ENST00000379328.7:c.829C>A | ENSP00000368632.3:p.Arg277= | 
            
              | ENST00000461472.1:n.443+5202C>A |  | 
            
              | XM_005252442.2:c.829C>A | XP_005252499.1:p.Arg277= | 
            
              | XM_005252443.3:c.829C>A | XP_005252500.1:p.Arg277= | 
            
              | XM_005252443.5:c.829C>A | XP_005252500.1:p.Arg277= |