| NM_003000.3:c.206G>T
                    
                              MANE Select | NP_002991.2:p.Gly69Val | 
            
              | ENST00000375499.8:c.206G>T
                    
                        MANE Select | ENSP00000364649.3:p.Gly69Val | 
            
              | NM_003000.2:c.206G>T , LRG_316t1:c.206G>T | NP_002991.2:p.Gly69Val | 
            
              | ENST00000375499.7:c.206G>T | ENSP00000364649.3:p.Gly69Val | 
            
              | ENST00000463045.2:c.35G>T | ENSP00000481376.1:p.Gly12Val | 
            
              | ENST00000463045.3:c.35G>T | ENSP00000481376.2:p.Gly12Val | 
            
              | ENST00000466613.2:n.218G>T |  | 
            
              | ENST00000475506.1:n.123G>T |  | 
            
              | ENST00000485515.5:n.194G>T |  | 
            
              | ENST00000491274.5:c.164G>T | ENSP00000480482.1:p.Gly55Val | 
            
              | ENST00000491274.6:c.164G>T | ENSP00000480482.2:p.Gly55Val |