Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
XM_017012910.1 | 108 | Intron | XP_016868399.1 | ||
XM_017012911.1 | 108 | Intron | XP_016868400.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000905.3 | 108 | Missense Mutation | CCG,CTG | P7L | NP_000896.1 |