| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_003884.4 | 223 | Missense Mutation | GCC,GGC | A51G | NP_003875.3 |
| XM_005265528.4 | 223 | Missense Mutation | GCC,GGC | A51G | XP_005265585.1 |
| XM_017007423.1 | 223 | Intron | XP_016862912.1 | ||
| XM_017007424.1 | 223 | Intron | XP_016862913.1 |