Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001144071.1 | 261 | Silent Mutation | CTG,TTG | L58L | NP_001137543.1 |
NM_144972.4 | 261 | Silent Mutation | CTG,TTG | L58L | NP_659409.2 |
XM_005252805.4 | 261 | Missense Mutation | CTG,TTG | L82L | XP_005252862.2 |
XM_011519922.2 | 261 | Missense Mutation | CTG,TTG | L82L | XP_011518224.1 |
XM_011519923.2 | 261 | Silent Mutation | CTG,TTG | L58L | XP_011518225.1 |
XM_011519924.2 | 261 | Missense Mutation | CTG,TTG | L58L | XP_011518226.1 |
XM_011519925.1 | 261 | Missense Mutation | CTG,TTG | L58L | XP_011518227.1 |