| NM_033380.3:c.1700G>C
                    
                              MANE Select | NP_203699.1:p.Gly567Ala | 
            
              | ENST00000328300.11:c.1700G>C
                    
                        MANE Select | ENSP00000331902.7:p.Gly567Ala | 
            
              | NM_000495.4:c.1700G>C | NP_000486.1:p.Gly567Ala | 
            
              | NM_000495.5:c.1700G>C | NP_000486.1:p.Gly567Ala | 
            
              | NM_033380.2:c.1700G>C | NP_203699.1:p.Gly567Ala | 
            
              | ENST00000328300.10:c.1700G>C | ENSP00000331902.6:p.Gly567Ala | 
            
              | ENST00000361603.6:c.1700G>C | ENSP00000354505.2:p.Gly567Ala | 
            
              | ENST00000361603.7:c.1700G>C | ENSP00000354505.2:p.Gly567Ala | 
            
              | ENST00000483338.1:n.1156G>C |  | 
            
              | XM_005262070.2:c.1700G>C | XP_005262127.1:p.Gly567Ala | 
            
              | XM_005262072.3:c.1700G>C | XP_005262129.1:p.Gly567Ala | 
            
              | XM_006724616.2:c.1700G>C | XP_006724679.1:p.Gly567Ala | 
            
              | XM_011530849.1:c.1376G>C | XP_011529151.1:p.Gly459Ala | 
            
              | XM_011530849.2:c.1715G>C | XP_011529151.2:p.Gly572Ala | 
            
              | XM_011530850.1:c.1700G>C | XP_011529152.1:p.Gly567Ala | 
            
              | XM_017029259.2:c.1715G>C | XP_016884748.1:p.Gly572Ala | 
            
              | XM_017029260.1:c.1715G>C | XP_016884749.1:p.Gly572Ala | 
            
              | XM_017029261.1:c.1715G>C | XP_016884750.1:p.Gly572Ala | 
            
              | XM_017029262.2:c.1715G>C | XP_016884751.1:p.Gly572Ala | 
            
              | XM_017029263.2:c.35G>C | XP_016884752.1:p.Gly12Ala |