| NM_000138.5:c.6559G>A
                    
                              MANE Select | NP_000129.3:p.Gly2187Ser | 
            
              | ENST00000316623.10:c.6559G>A
                    
                        MANE Select | ENSP00000325527.5:p.Gly2187Ser | 
            
              | NM_000138.4:c.6559G>A , LRG_778t1:c.6559G>A | NP_000129.3:p.Gly2187Ser | 
            
              | ENST00000316623.9:c.6559G>A | ENSP00000325527.5:p.Gly2187Ser | 
            
              | ENST00000537463.6:c.*2322G>A | ENSP00000440294.2:n.*2322G>A | 
            
              | ENST00000559133.5:c.1866G>A |  | 
            
              | ENST00000559133.6:c.6559G>A | ENSP00000453958.2:p.Gly2187Ser | 
            
              | ENST00000674301.1:c.1558G>A | ENSP00000501333.1:p.Gly520Ser | 
            
              | ENST00000674301.2:c.6559G>A | ENSP00000501333.2:p.Gly2187Ser | 
            
              | ENST00000682170.1:n.168G>A |  |