| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_006785.3 | 521 | Missense Mutation | CCC,CTC | P88L | NP_006776.1 |
| NM_173844.2 | 521 | Missense Mutation | CCC,CTC | P88L | NP_776216.1 |
| XM_011525794.1 | 521 | Missense Mutation | CCC,CTC | P88L | XP_011524096.1 |