| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000431.3 | 262 | Missense Mutation | CCC,CTC | P39L | NP_000422.1 |
| NM_001114185.2 | 262 | Missense Mutation | CCC,CTC | P39L | NP_001107657.1 |
| NM_001301182.1 | 262 | Missense Mutation | CCC,CTC | P39L | NP_001288111.1 |
| XM_011538372.2 | 262 | Missense Mutation | CCC,CTC | P139L | XP_011536674.2 |
| XM_017019313.1 | 262 | Missense Mutation | CCC,CTC | P39L | XP_016874802.1 |
| XM_017019314.1 | 262 | Missense Mutation | CCC,CTC | P39L | XP_016874803.1 |