| NM_004360.5:c.2310C>G
                    
                              MANE Select | NP_004351.1:p.Ser770Arg | 
            
              | ENST00000261769.10:c.2310C>G
                    
                        MANE Select | ENSP00000261769.4:p.Ser770Arg | 
            
              | NM_001317184.1:c.2127C>G | NP_001304113.1:p.Ser709Arg | 
            
              | NM_001317184.2:c.2127C>G | NP_001304113.1:p.Ser709Arg | 
            
              | NM_001317185.1:c.762C>G | NP_001304114.1:p.Ser254Arg | 
            
              | NM_001317185.2:c.762C>G | NP_001304114.1:p.Ser254Arg | 
            
              | NM_001317186.1:c.345C>G | NP_001304115.1:p.Ser115Arg | 
            
              | NM_001317186.2:c.345C>G | NP_001304115.1:p.Ser115Arg | 
            
              | NM_004360.3:c.2310C>G , LRG_301t1:c.2310C>G | NP_004351.1:p.Ser770Arg | 
            
              | NM_004360.4:c.2310C>G | NP_004351.1:p.Ser770Arg | 
            
              | ENST00000261769.9:c.2310C>G | ENSP00000261769.4:p.Ser770Arg | 
            
              | ENST00000422392.6:c.2127C>G | ENSP00000414946.2:p.Ser709Arg | 
            
              | ENST00000562118.1:n.528C>G |  | 
            
              | ENST00000562836.5:n.2381C>G |  | 
            
              | ENST00000566510.5:c.*976C>G | ENSP00000458139.1:n.*976C>G | 
            
              | ENST00000566612.5:c.*550C>G | ENSP00000454782.1:n.*550C>G | 
            
              | ENST00000611625.4:c.2373C>G | ENSP00000481063.1:p.Ser791Arg | 
            
              | ENST00000612417.4:c.1853+3114C>G | ENSP00000478360.1:n.1853+3114C>G | 
            
              | ENST00000621016.4:c.1866-4535C>G | ENSP00000480664.1:n.1866-4535C>G | 
            
              | XM_011523488.1:c.1575C>G | XP_011521790.1:p.Ser525Arg | 
            
              | XM_011523489.1:c.1575C>G | XP_011521791.1:p.Ser525Arg |