| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_013268.2 | 216 | Missense Mutation | GGC,GTC | G59V | NP_037400.1 |
| XM_011526874.2 | 216 | Missense Mutation | GGC,GTC | G52V | XP_011525176.1 |
| XM_017026715.1 | 216 | Missense Mutation | GGC,GTC | G90V | XP_016882204.1 |