| NM_005236.3:c.2537C=
                    
                              MANE Select | NP_005227.1:p.Pro846= | 
            
              | ENST00000311895.8:c.2537C=
                    
                        MANE Select | ENSP00000310520.7:p.Pro846= | 
            
              | NM_005236.2:c.2537C= , LRG_463t1:c.2537C= | NP_005227.1:p.Pro846= | 
            
              | ENST00000311895.7:c.2537C= | ENSP00000310520.7:p.Pro846= | 
            
              | ENST00000389138.7:n.1814C= |  | 
            
              | ENST00000682617.1:c.2675C= | ENSP00000507912.1:p.Pro892= | 
            
              | ENST00000683962.1:c.*2231C= | ENSP00000506854.1:n.*2231C= | 
            
              | XM_011522424.1:c.2675C= | XP_011520726.1:p.Pro892= | 
            
              | XM_011522424.3:c.2675C= | XP_011520726.1:p.Pro892= | 
            
              | XM_011522425.1:c.1994C= | XP_011520727.1:p.Pro665= | 
            
              | XM_011522426.1:c.1748C= | XP_011520728.1:p.Pro583= | 
            
              | XM_011522427.1:c.1187C= | XP_011520729.1:p.Pro396= | 
            
              | XM_017023043.2:c.1748C= | XP_016878532.1:p.Pro583= | 
            
              | XR_932805.1:n.2696C= |  |