Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_016246.2 | 998 | Silent Mutation | CTC,CTT | L244L | NP_057330.2 |
XM_005258969.3 | 998 | Missense Mutation | TCG,TTG | S212L | XP_005259026.1 |
XM_005258970.3 | 998 | UTR 3 | XP_005259027.1 |