| NM_000507.4:c.960A=
                    
                              MANE Select | NP_000498.2:p.Gly320= | 
            
              | ENST00000375326.9:c.960A=
                    
                        MANE Select | ENSP00000364475.5:p.Gly320= | 
            
              | NM_000507.3:c.960A= | NP_000498.2:p.Gly320= | 
            
              | NM_001127628.1:c.960A= | NP_001121100.1:p.Gly320= | 
            
              | NM_001127628.2:c.960A= | NP_001121100.1:p.Gly320= | 
            
              | ENST00000375326.8:c.960A= | ENSP00000364475.4:p.Gly320= | 
            
              | ENST00000415431.5:c.960A= | ENSP00000408025.1:p.Gly320= | 
            
              | ENST00000648117.1:c.765A= | ENSP00000498145.1:p.Gly255= | 
            
              | ENST00000682520.1:c.1120A= | ENSP00000507547.1:n.1120A= | 
            
              | XM_006717005.2:c.714A= | XP_006717068.1:p.Gly238= | 
            
              | XM_006717005.4:c.714A= | XP_006717068.1:p.Gly238= |