| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_003803.3 | 4902 | Missense Mutation | GCC,GTC | A1614V | NP_003794.3 |
| NM_019856.1 | 4902 | Missense Mutation | GCC,GTC | A1518V | NP_062830.1 |
| XM_017026062.1 | 4902 | Missense Mutation | GCC,GTC | A1602V | XP_016881551.1 |