| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001270780.1 | 657 | Intron | NP_001257709.1 | ||
| NM_001270781.1 | 657 | Intron | NP_001257710.1 | ||
| NM_033423.4 | 657 | Missense Mutation | ACT,CCT | T184P | NP_219491.1 |
| XM_011536683.2 | 657 | Missense Mutation | ACT,CCT | T150P | XP_011534985.1 |