Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001199295.1 | 661 | Missense Mutation | ATG,TTG | M113L | NP_001186224.1 |
NM_153263.2 | 661 | Missense Mutation | ATG,TTG | M100L | NP_694995.2 |
XM_006723128.3 | 661 | Missense Mutation | ATG,TTG | M91L | XP_006723191.1 |