| NM_000540.3:c.6847A>C
                    
                              MANE Select | NP_000531.2:p.Asn2283His | 
            
              | ENST00000359596.8:c.6847A>C
                    
                        MANE Select | ENSP00000352608.2:p.Asn2283His | 
            
              | NM_000540.2:c.6847A>C , LRG_766t1:c.6847A>C | NP_000531.2:p.Asn2283His | 
            
              | NM_001042723.1:c.6847A>C | NP_001036188.1:p.Asn2283His | 
            
              | NM_001042723.2:c.6847A>C | NP_001036188.1:p.Asn2283His | 
            
              | ENST00000355481.8:c.6847A>C | ENSP00000347667.3:p.Asn2283His | 
            
              | ENST00000359596.7:c.6847A>C | ENSP00000352608.2:p.Asn2283His | 
            
              | ENST00000360985.7:c.6844A>C | ENSP00000354254.4:p.Asn2282His | 
            
              | ENST00000594335.5:c.299A>C |  | 
            
              | ENST00000599547.6:c.6847A>C | ENSP00000471601.2:p.Asn2283His | 
            
              | XM_006723317.1:c.6847A>C | XP_006723380.1:p.Asn2283His | 
            
              | XM_006723317.2:c.6847A>C | XP_006723380.1:p.Asn2283His | 
            
              | XM_006723319.1:c.6847A>C | XP_006723382.1:p.Asn2283His | 
            
              | XM_006723319.2:c.6847A>C | XP_006723382.1:p.Asn2283His | 
            
              | XM_011527204.1:c.6844A>C | XP_011525506.1:p.Asn2282His | 
            
              | XM_011527205.1:c.6847A>C | XP_011525507.1:p.Asn2283His | 
            
              | XM_011527205.2:c.6847A>C | XP_011525507.1:p.Asn2283His | 
            
              | XR_001753735.1:n.6930A>C |  |