Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_207359.2 | 1467 | Missense Mutation | ATG,TTG | M474L | NP_997242.2 |
XM_017006297.1 | 1467 | Missense Mutation | ATG,TTG | M455L | XP_016861786.1 |
XM_017006298.1 | 1467 | Missense Mutation | ATG,TTG | M228L | XP_016861787.1 |