| NM_000817.3:c.638+62A>G
                    
                              MANE Select | NP_000808.2:n.638+62A>G | 
            
              | ENST00000358196.8:c.638+62A>G
                    
                        MANE Select | ENSP00000350928.3:n.638+62A>G | 
            
              | NM_000817.2:c.638+62A>G | NP_000808.2:n.638+62A>G | 
            
              | NM_013445.3:c.638+62A>G | NP_038473.2:n.638+62A>G | 
            
              | NM_013445.4:c.638+62A>G | NP_038473.2:n.638+62A>G | 
            
              | ENST00000344257.9:c.638+62A>G | ENSP00000341167.5:n.638+62A>G | 
            
              | ENST00000358196.7:c.638+62A>G | ENSP00000350928.3:n.638+62A>G | 
            
              | ENST00000375272.5:c.638+62A>G | ENSP00000364421.1:n.638+62A>G | 
            
              | ENST00000414527.6:c.638+62A>G | ENSP00000403849.1:n.638+62A>G | 
            
              | ENST00000429023.1:n.619+62A>G |  | 
            
              | ENST00000493875.5:c.638+62A>G | ENSP00000434696.1:n.638+62A>G | 
            
              | ENST00000625689.2:c.638+62A>G | ENSP00000486612.1:n.638+62A>G | 
            
              | XM_005246444.2:c.638+62A>G | XP_005246501.1:n.638+62A>G | 
            
              | XM_005246444.3:c.638+62A>G | XP_005246501.1:n.638+62A>G | 
            
              | XM_011510922.1:c.638+62A>G | XP_011509224.1:n.638+62A>G | 
            
              | XM_017003756.1:c.638+62A>G | XP_016859245.1:n.638+62A>G | 
            
              | XM_017003757.2:c.638+62A>G | XP_016859246.1:n.638+62A>G | 
            
              | XM_017003758.2:c.638+62A>G | XP_016859247.1:n.638+62A>G |