| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001098200.1 | 1238 | Missense Mutation | ACG,ATG | T246M | NP_001091670.1 |
| NM_005292.3 | 1238 | Missense Mutation | ACG,ATG | T246M | NP_005283.1 |
| XM_006719946.3 | 1238 | Missense Mutation | ACG,ATG | T246M | XP_006720009.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001144072.1 | 1238 | Intron | NP_001137544.1 | ||
| NM_177967.3 | 1238 | Intron | NP_808882.1 | ||
| XM_006719948.3 | 1238 | Intron | XP_006720011.1 | ||
| XM_011521082.2 | 1238 | Intron | XP_011519384.1 | ||
| XM_011521083.2 | 1238 | Intron | XP_011519385.1 | ||
| XM_011521084.2 | 1238 | Intron | XP_011519386.1 | ||
| XM_017020553.1 | 1238 | Intron | XP_016876042.1 |