| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_003386.2 | 503 | Missense Mutation | GCC,GGC | A113G | NP_003377.2 |
| NM_173059.2 | 503 | Missense Mutation | GCC,GGC | A113G | NP_775082.2 |
| XM_011516555.2 | 503 | Missense Mutation | GCC,GGC | A113G | XP_011514857.1 |
| XM_017012581.1 | 503 | Intron | XP_016868070.1 |