| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001167579.1 | 321 | Missense Mutation | CCC,GCC | P92A | NP_001161051.1 |
| NM_003052.4 | 321 | Missense Mutation | CCC,GCC | P92A | NP_003043.3 |
| XM_005265975.1 | 321 | Missense Mutation | CCC,GCC | P92A | XP_005266032.1 |
| XM_017009773.1 | 321 | Missense Mutation | CCC,GCC | P92A | XP_016865262.1 |
| XM_017009774.1 | 321 | Intron | XP_016865263.1 | ||
| XM_017009775.1 | 321 | Missense Mutation | CCC,GCC | P92A | XP_016865264.1 |