| NM_000428.3:c.804G>A
                    
                              MANE Select | NP_000419.1:p.Pro268= | 
            
              | ENST00000261978.9:c.804G>A
                    
                        MANE Select | ENSP00000261978.4:p.Pro268= | 
            
              | NM_000428.2:c.804G>A | NP_000419.1:p.Pro268= | 
            
              | ENST00000261978.8:c.804G>A | ENSP00000261978.4:p.Pro268= | 
            
              | ENST00000553939.5:c.804G>A | ENSP00000452110.1:p.Pro268= | 
            
              | ENST00000556690.5:c.804G>A | ENSP00000451477.1:p.Pro268= | 
            
              | ENST00000557425.1:n.123+26166G>A |  | 
            
              | XM_011536765.1:c.804G>A | XP_011535067.1:p.Pro268= | 
            
              | XM_011536765.2:c.804G>A | XP_011535067.1:p.Pro268= | 
            
              | XM_011536766.1:c.345G>A | XP_011535068.1:p.Pro115= | 
            
              | XM_011536767.1:c.321G>A | XP_011535069.1:p.Pro107= |