| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001033714.2 | 2399 | Missense Mutation | CCA,GCA | P757A | NP_001028886.1 |
| NM_001258308.1 | 2399 | Missense Mutation | CCA,GCA | P761A | NP_001245237.1 |
| NM_001258309.1 | 2399 | Missense Mutation | CCA,GCA | P794A | NP_001245238.1 |
| NM_001258310.1 | 2399 | UTR 3 | NP_001245239.1 | ||
| NM_006170.3 | 2399 | Missense Mutation | CCA,GCA | P757A | NP_006161.2 |
| XM_005253691.1 | 2399 | Missense Mutation | CCA,GCA | P761A | XP_005253748.1 |