| NM_000483.5:c.238G>T
                  (APOC2)
                    
                              MANE Select | NP_000474.2:p.Ala80Ser | 
            
              | ENST00000252490.7:c.238G>T
                  (APOC2)
                    
                        MANE Select | ENSP00000252490.5:p.Ala80Ser | 
            
              | NM_000483.4:c.238G>T
                  (APOC2) | NP_000474.2:p.Ala80Ser | 
            
              | NR_037932.1:n.1445G>T
                  (APOC4-APOC2) |  | 
            
              | ENST00000252490.5:c.238G>T
                  (APOC4-APOC2) | ENSP00000252490.4:p.Ala80Ser | 
            
              | ENST00000585685.5:c.*1021G>T
                  (APOC4-APOC2) | ENSP00000467185.1:n.*1021G>T | 
            
              | ENST00000585786.1:c.*317G>T
                  (APOC2) | ENSP00000465001.1:n.*317G>T | 
            
              | ENST00000589057.5:c.469G>T
                  (APOC4-APOC2) | ENSP00000468139.1:p.Ala157Ser | 
            
              | ENST00000590360.2:c.238G>T
                  (APOC2) | ENSP00000466775.1:p.Ala80Ser | 
            
              | ENST00000591597.5:c.196G>T
                  (APOC2) | ENSP00000476835.1:p.Ala66Ser | 
            
              | ENST00000592257.5:c.*32G>T
                  (APOC2) | ENSP00000477261.1:n.*32G>T |