| NM_016341.4:c.5240C>G
                    
                              MANE Select | NP_057425.3:p.Ala1747Gly | 
            
              | ENST00000371380.8:c.5240C>G
                    
                        MANE Select | ENSP00000360431.2:p.Ala1747Gly | 
            
              | NM_001165979.2:c.4316C>G | NP_001159451.1:p.Ala1439Gly | 
            
              | NM_001288989.1:c.5192C>G | NP_001275918.1:p.Ala1731Gly | 
            
              | NM_001288989.2:c.5192C>G | NP_001275918.1:p.Ala1731Gly | 
            
              | NM_016341.3:c.5240C>G | NP_057425.3:p.Ala1747Gly | 
            
              | ENST00000260766.7:c.5240C>G | ENSP00000260766.3:p.Ala1747Gly | 
            
              | ENST00000371375.1:c.4316C>G | ENSP00000360426.1:p.Ala1439Gly | 
            
              | ENST00000371375.2:c.4316C>G | ENSP00000360426.1:p.Ala1439Gly | 
            
              | ENST00000371380.7:c.5240C>G | ENSP00000360431.2:p.Ala1747Gly | 
            
              | ENST00000371385.7:c.4316C>G | ENSP00000360438.3:p.Ala1439Gly | 
            
              | ENST00000371385.8:c.4214C>G | ENSP00000360438.4:p.Ala1405Gly | 
            
              | ENST00000674738.1:c.3795C>G |  | 
            
              | ENST00000674827.1:c.3356C>G | ENSP00000502523.1:p.Ala1119Gly | 
            
              | ENST00000675218.1:c.4316C>G | ENSP00000501910.1:p.Ala1439Gly | 
            
              | ENST00000675487.1:c.*1173C>G | ENSP00000502340.1:n.*1173C>G | 
            
              | ENST00000675718.1:c.4509C>G |  | 
            
              | ENST00000676102.1:c.4085C>G | ENSP00000502811.1:p.Ala1362Gly | 
            
              | ENST00000685253.1:c.*1783C>G | ENSP00000509405.1:n.*1783C>G | 
            
              | ENST00000685889.1:n.1975C>G |  | 
            
              | ENST00000686807.1:n.659C>G |  | 
            
              | ENST00000686954.1:c.*524C>G | ENSP00000508416.1:n.*524C>G | 
            
              | ENST00000688810.1:c.4268C>G | ENSP00000509140.1:p.Ala1423Gly | 
            
              | ENST00000689233.1:n.9448C>G |  | 
            
              | ENST00000690340.1:n.2913C>G |  | 
            
              | ENST00000692286.1:c.5108C>G | ENSP00000509490.1:p.Ala1703Gly | 
            
              | ENST00000692396.1:c.5192C>G | ENSP00000508605.1:p.Ala1731Gly | 
            
              | XM_006717885.2:c.5282C>G | XP_006717948.1:p.Ala1761Gly | 
            
              | XM_006717885.4:c.5282C>G | XP_006717948.1:p.Ala1761Gly | 
            
              | XM_006717886.2:c.5282C>G | XP_006717949.1:p.Ala1761Gly | 
            
              | XM_006717888.2:c.5279C>G | XP_006717951.1:p.Ala1760Gly | 
            
              | XM_006717888.4:c.5279C>G | XP_006717951.1:p.Ala1760Gly | 
            
              | XM_006717889.2:c.5234C>G | XP_006717952.1:p.Ala1745Gly | 
            
              | XM_006717889.4:c.5234C>G | XP_006717952.1:p.Ala1745Gly | 
            
              | XM_006717890.1:c.4358C>G | XP_006717953.1:p.Ala1453Gly | 
            
              | XM_006717890.3:c.4358C>G | XP_006717953.1:p.Ala1453Gly | 
            
              | XM_011539849.1:c.5282C>G | XP_011538151.1:p.Ala1761Gly | 
            
              | XM_011539849.3:c.5282C>G | XP_011538151.1:p.Ala1761Gly | 
            
              | XM_011539850.1:c.4127C>G | XP_011538152.1:p.Ala1376Gly | 
            
              | XM_011539850.3:c.4127C>G | XP_011538152.1:p.Ala1376Gly | 
            
              | XM_017016310.2:c.5282C>G | XP_016871799.1:p.Ala1761Gly | 
            
              | XM_017016311.2:c.5282C>G | XP_016871800.1:p.Ala1761Gly | 
            
              | XM_017016312.2:c.4268C>G | XP_016871801.1:p.Ala1423Gly |