| NM_006030.4:c.816C>A
                    
                              MANE Select | NP_006021.2:p.Asp272Glu | 
            
              | ENST00000424201.7:c.816C>A
                    
                        MANE Select | ENSP00000390329.2:p.Asp272Glu | 
            
              | NM_001005505.2:c.816C>A | NP_001005505.1:p.Asp272Glu | 
            
              | NM_001005505.3:c.816C>A | NP_001005505.1:p.Asp272Glu | 
            
              | NM_001174051.2:c.816C>A | NP_001167522.1:p.Asp272Glu | 
            
              | NM_001174051.3:c.816C>A | NP_001167522.1:p.Asp272Glu | 
            
              | NM_001291101.1:c.609C>A | NP_001278030.1:p.Asp203Glu | 
            
              | NM_006030.3:c.816C>A | NP_006021.2:p.Asp272Glu | 
            
              | ENST00000266039.7:c.816C>A | ENSP00000266039.3:p.Asp272Glu | 
            
              | ENST00000360963.7:c.609C>A | ENSP00000354228.3:p.Asp203Glu | 
            
              | ENST00000423994.6:c.816C>A | ENSP00000407393.2:p.Asp272Glu | 
            
              | ENST00000424201.6:c.816C>A | ENSP00000390329.2:p.Asp272Glu | 
            
              | ENST00000429770.5:c.816C>A | ENSP00000404631.1:p.Asp272Glu | 
            
              | ENST00000479441.1:c.816C>A | ENSP00000418081.1:p.Asp272Glu | 
            
              | XM_005265581.3:c.816C>A | XP_005265638.1:p.Asp272Glu | 
            
              | XM_005265581.4:c.816C>A | XP_005265638.1:p.Asp272Glu | 
            
              | XM_011534242.1:c.816C>A | XP_011532544.1:p.Asp272Glu | 
            
              | XM_011534243.1:c.816C>A | XP_011532545.1:p.Asp272Glu | 
            
              | XM_011534243.2:c.816C>A | XP_011532545.1:p.Asp272Glu | 
            
              | XM_011534244.1:c.816C>A | XP_011532546.1:p.Asp272Glu |