| NM_025099.6:c.534C>G
                    
                              MANE Select | NP_079375.3:p.His178Gln | 
            
              | ENST00000651323.1:c.534C>G
                    
                        MANE Select | ENSP00000498499.1:p.His178Gln | 
            
              | NM_025099.5:c.534C>G | NP_079375.3:p.His178Gln | 
            
              | NR_046431.1:n.593C>G |  | 
            
              | NR_046431.2:n.554C>G |  | 
            
              | ENST00000315684.12:c.534C>G | ENSP00000313759.8:p.His178Gln | 
            
              | ENST00000449476.6:c.534C>G | ENSP00000396018.2:p.His178Gln | 
            
              | ENST00000449476.7:c.534C>G | ENSP00000396018.2:p.His178Gln | 
            
              | ENST00000580299.2:c.534C>G | ENSP00000462607.2:p.His178Gln | 
            
              | ENST00000581671.1:n.375C>G |  | 
            
              | ENST00000581671.2:n.375C>G |  | 
            
              | ENST00000581729.2:c.534C>G | ENSP00000462720.2:p.His178Gln | 
            
              | ENST00000581967.2:n.556C>G |  | 
            
              | ENST00000643543.1:c.534C>G | ENSP00000494323.1:p.His178Gln | 
            
              | ENST00000699849.1:c.-364C>G | ENSP00000514647.1:n.-364C>G | 
            
              | ENST00000699850.1:n.56-1802C>G |  | 
            
              | ENST00000699851.1:n.556C>G |  | 
            
              | ENST00000699852.1:c.534C>G | ENSP00000514648.1:p.His178Gln | 
            
              | ENST00000699853.1:c.534C>G | ENSP00000514649.1:p.His178Gln | 
            
              | ENST00000699854.1:n.327C>G |  | 
            
              | ENST00000699855.1:n.556C>G |  | 
            
              | ENST00000699856.1:c.534C>G | ENSP00000514650.1:p.His178Gln | 
            
              | ENST00000699857.1:n.542C>G |  | 
            
              | ENST00000699858.1:c.534C>G | ENSP00000514651.1:p.His178Gln | 
            
              | ENST00000699859.1:c.534C>G | ENSP00000514652.1:p.His178Gln | 
            
              | ENST00000699861.1:n.556C>G |  | 
            
              | ENST00000699862.1:n.421C>G |  | 
            
              | XM_006721577.2:c.534C>G | XP_006721640.1:p.His178Gln | 
            
              | XM_006721577.3:c.534C>G | XP_006721640.1:p.His178Gln | 
            
              | XM_006721578.2:c.534C>G | XP_006721641.1:p.His178Gln | 
            
              | XM_006721578.3:c.534C>G | XP_006721641.1:p.His178Gln | 
            
              | XM_006721579.2:c.534C>G | XP_006721642.1:p.His178Gln | 
            
              | XM_011524010.1:c.534C>G | XP_011522312.1:p.His178Gln | 
            
              | XM_011524010.2:c.534C>G | XP_011522312.1:p.His178Gln | 
            
              | XM_011524011.1:c.-255+248C>G | XP_011522313.1:n.-255+248C>G | 
            
              | XM_011524011.2:c.-255+248C>G | XP_011522313.1:n.-255+248C>G | 
            
              | XR_001752639.1:n.577C>G |  | 
            
              | XR_001752640.1:n.577C>G |  | 
            
              | XR_001752641.1:n.577C>G |  | 
            
              | XR_001752642.1:n.577C>G |  | 
            
              | XR_001752643.1:n.577C>G |  | 
            
              | XR_001752644.1:n.577C>G |  | 
            
              | XR_002958073.1:n.577C>G |  | 
            
              | XR_429823.2:n.577C>G |  | 
            
              | XR_429823.3:n.577C>G |  | 
            
              | XR_429824.2:n.577C>G |  | 
            
              | XR_429824.3:n.577C>G |  | 
            
              | XR_429825.1:n.577C>G |  |