Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001008801.1 | 994 | Intron | NP_001008801.1 | ||
NM_001277120.1 | 994 | Intron | NP_001264049.1 | ||
XM_017027443.1 | 994 | Missense Mutation | ATG,CTG | M229L | XP_016882932.1 |
XM_017027444.1 | 994 | Missense Mutation | ATG,CTG | M157L | XP_016882933.1 |