| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_019002.3 | 266 | Missense Mutation | CCC,CTC | P45L | NP_061875.2 |
| XM_017004376.1 | 266 | Missense Mutation | CCC,CTC | P45L | XP_016859865.1 |
| XM_017004377.1 | 266 | Missense Mutation | CCC,CTC | P45L | XP_016859866.1 |