| NM_000669.5:c.1104-222G>A
                  (ADH1C)
                    
                              MANE Select | NP_000660.1:n.1104-222G>A | 
            
              | ENST00000515683.6:c.1104-222G>A
                  (ADH1C)
                    
                        MANE Select | ENSP00000426083.1:n.1104-222G>A | 
            
              | NM_000669.4:c.1104-222G>A
                  (ADH1C) | NP_000660.1:n.1104-222G>A | 
            
              | NR_133005.1:n.1430-222G>A
                  (ADH1C) |  | 
            
              | NR_133005.2:n.1131-222G>A
                  (ADH1C) |  | 
            
              | ENST00000515683.5:c.1104-222G>A
                  (ADH1C) | ENSP00000426083.1:n.1104-222G>A | 
            
              | ENST00000639454.1:c.18+15660G>A
                  (ADH1B) | ENSP00000491622.1:n.18+15660G>A | 
            
              | XM_011531588.1:c.1002-222G>A
                  (ADH1C) | XP_011529890.1:n.1002-222G>A | 
            
              | XM_011531589.1:c.984-222G>A
                  (ADH1C) | XP_011529891.1:n.984-222G>A |