| NM_000817.3:c.1263+128A=
                    
                              MANE Select | NP_000808.2:n.1263+128A= | 
            
              | ENST00000358196.8:c.1263+128A=
                    
                        MANE Select | ENSP00000350928.3:n.1263+128A= | 
            
              | NM_000817.2:c.1263+128A= | NP_000808.2:n.1263+128A= | 
            
              | ENST00000358196.7:c.1263+128A= | ENSP00000350928.3:n.1263+128A= | 
            
              | ENST00000414527.6:c.*448+128A= | ENSP00000403849.1:n.*448+128A= | 
            
              | ENST00000478562.1:n.433A= |  | 
            
              | ENST00000488724.5:n.363+128A= |  | 
            
              | ENST00000493875.5:c.*97+128A= | ENSP00000434696.1:n.*97+128A= | 
            
              | ENST00000625689.2:c.*97+128A= | ENSP00000486612.1:n.*97+128A= | 
            
              | XM_011510922.1:c.1263+128A= | XP_011509224.1:n.1263+128A= | 
            
              | XM_017003756.1:c.1263+128A= | XP_016859245.1:n.1263+128A= | 
            
              | XM_024452783.1:c.495+128A= | XP_024308551.1:n.495+128A= |