| NM_000484.4:c.1995G>T
                    
                              MANE Select | NP_000475.1:p.Glu665Asp | 
            
              | ENST00000346798.8:c.1995G>T
                    
                        MANE Select | ENSP00000284981.4:p.Glu665Asp | 
            
              | NM_000484.3:c.1995G>T | NP_000475.1:p.Glu665Asp | 
            
              | NM_001136016.3:c.1923G>T | NP_001129488.1:p.Glu641Asp | 
            
              | NM_001136129.2:c.1602G>T | NP_001129601.1:p.Glu534Asp | 
            
              | NM_001136129.3:c.1602G>T | NP_001129601.1:p.Glu534Asp | 
            
              | NM_001136130.2:c.1827G>T | NP_001129602.1:p.Glu609Asp | 
            
              | NM_001136130.3:c.1827G>T | NP_001129602.1:p.Glu609Asp | 
            
              | NM_001136131.2:c.1665G>T | NP_001129603.1:p.Glu555Asp | 
            
              | NM_001136131.3:c.1665G>T | NP_001129603.1:p.Glu555Asp | 
            
              | NM_001204301.1:c.1941G>T | NP_001191230.1:p.Glu647Asp | 
            
              | NM_001204301.2:c.1941G>T | NP_001191230.1:p.Glu647Asp | 
            
              | NM_001204302.1:c.1884G>T | NP_001191231.1:p.Glu628Asp | 
            
              | NM_001204302.2:c.1884G>T | NP_001191231.1:p.Glu628Asp | 
            
              | NM_001204303.1:c.1716G>T | NP_001191232.1:p.Glu572Asp | 
            
              | NM_001204303.2:c.1716G>T | NP_001191232.1:p.Glu572Asp | 
            
              | NM_001385253.1:c.1827G>T | NP_001372182.1:p.Glu609Asp | 
            
              | NM_201413.2:c.1938G>T | NP_958816.1:p.Glu646Asp | 
            
              | NM_201413.3:c.1938G>T | NP_958816.1:p.Glu646Asp | 
            
              | NM_201414.2:c.1770G>T | NP_958817.1:p.Glu590Asp | 
            
              | NM_201414.3:c.1770G>T | NP_958817.1:p.Glu590Asp | 
            
              | ENST00000346798.7:c.1995G>T | ENSP00000284981.4:p.Glu665Asp | 
            
              | ENST00000348990.9:c.1770G>T | ENSP00000345463.5:p.Glu590Asp | 
            
              | ENST00000354192.7:c.1602G>T | ENSP00000346129.3:p.Glu534Asp | 
            
              | ENST00000357903.7:c.1938G>T | ENSP00000350578.3:p.Glu646Asp | 
            
              | ENST00000358918.7:c.1941G>T | ENSP00000351796.3:p.Glu647Asp | 
            
              | ENST00000359726.7:c.1665G>T | ENSP00000352760.4:p.Glu555Asp | 
            
              | ENST00000439274.6:c.1827G>T | ENSP00000398879.2:p.Glu609Asp | 
            
              | ENST00000440126.7:c.1923G>T | ENSP00000387483.2:p.Glu641Asp | 
            
              | ENST00000464867.1:n.342G>T |  | 
            
              | ENST00000707132.1:n.1962G>T |  | 
            
              | ENST00000707133.1:n.392G>T |  | 
            
              | ENST00000707134.1:n.661G>T |  |