| NM_005343.4:c.37G>T
                  (HRAS)
                    
                              MANE Select | NP_005334.1:p.Gly13Cys | 
            
              | ENST00000311189.8:c.37G>T
                  (HRAS)
                    
                        MANE Select | ENSP00000309845.7:p.Gly13Cys | 
            
              | NM_176795.5:c.37G>T
                  (HRAS)
                    
                              MANE Plus Clinical | NP_789765.1:p.Gly13Cys | 
            
              | ENST00000417302.7:c.37G>T
                  (HRAS)
                    
                        MANE Plus Clinical | ENSP00000388246.1:p.Gly13Cys | 
            
              | NM_001130442.1:c.37G>T
                  (HRAS) | NP_001123914.1:p.Gly13Cys | 
            
              | NM_001130442.2:c.37G>T
                  (HRAS) | NP_001123914.1:p.Gly13Cys | 
            
              | NM_001130442.3:c.37G>T
                  (HRAS) | NP_001123914.1:p.Gly13Cys | 
            
              | NM_001318054.1:c.-283G>T
                  (HRAS) | NP_001304983.1:n.-283G>T | 
            
              | NM_001318054.2:c.-283G>T
                  (HRAS) | NP_001304983.1:n.-283G>T | 
            
              | NM_005343.2:c.37G>T
                  (HRAS) | NP_005334.1:p.Gly13Cys | 
            
              | NM_005343.3:c.37G>T
                  (HRAS) | NP_005334.1:p.Gly13Cys | 
            
              | NM_176795.3:c.37G>T
                  (HRAS) | NP_789765.1:p.Gly13Cys | 
            
              | NM_176795.4:c.37G>T
                  (HRAS) | NP_789765.1:p.Gly13Cys | 
            
              | ENST00000311189.7:c.37G>T
                  (HRAS) | ENSP00000309845.7:p.Gly13Cys | 
            
              | ENST00000397594.5:c.37G>T
                  (HRAS) | ENSP00000380722.1:p.Gly13Cys | 
            
              | ENST00000397594.7:c.37G>T
                  (HRAS) | ENSP00000380722.3:p.Gly13Cys | 
            
              | ENST00000397596.6:c.37G>T
                  (HRAS) | ENSP00000380723.2:p.Gly13Cys | 
            
              | ENST00000417302.5:c.37G>T
                  (HRAS) | ENSP00000388246.1:p.Gly13Cys | 
            
              | ENST00000417302.6:c.37G>T
                  (HRAS) | ENSP00000388246.1:p.Gly13Cys | 
            
              | ENST00000451590.5:c.37G>T
                  (HRAS) | ENSP00000407586.1:p.Gly13Cys | 
            
              | ENST00000462734.2:c.37G>T
                  (HRAS) | ENSP00000507303.1:p.Gly13Cys | 
            
              | ENST00000468682.2:n.525G>T
                  (HRAS) |  | 
            
              | ENST00000482021.1:n.160G>T
                  (HRAS) |  | 
            
              | ENST00000493230.5:c.37G>T
                  (HRAS) | ENSP00000434023.1:p.Gly13Cys | 
            
              | XM_011519875.1:c.-424-4312C>A
                  (LRRC56) | XP_011518177.1:n.-424-4312C>A | 
            
              | XM_011519875.2:c.-424-4312C>A
                  (LRRC56) | XP_011518177.1:n.-424-4312C>A | 
            
              | XM_011519877.1:c.-161-5294C>A
                  (LRRC56) | XP_011518179.1:n.-161-5294C>A | 
            
              | XM_011519877.2:c.-161-5294C>A
                  (LRRC56) | XP_011518179.1:n.-161-5294C>A | 
            
              | XM_017017167.1:c.-499-4237C>A
                  (LRRC56) | XP_016872656.1:n.-499-4237C>A | 
            
              | XM_017017168.1:c.-499-4237C>A
                  (LRRC56) | XP_016872657.1:n.-499-4237C>A | 
            
              | XR_242795.1:n.236G>T
                  (HRAS) |  |