Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001128202.2 | 489 | Intron | NP_001121674.1 | ||
NM_001318133.1 | 489 | Missense Mutation | ACC,GCC | T112A | NP_001305062.1 |
XM_005269817.4 | 489 | Intron | XP_005269874.1 |