| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001206612.1 | 502 | Missense Mutation | ATG,ATT | M41I | NP_001193541.1 |
| NM_001244664.1 | 502 | Missense Mutation | ATG,ATT | M41I | NP_001231593.1 |
| NM_001317077.1 | 502 | Missense Mutation | ATG,ATT | M41I | NP_001304006.1 |
| NM_015607.3 | 502 | Missense Mutation | ATG,ATT | M41I | NP_056422.2 |
| XM_017000993.1 | 502 | Missense Mutation | ATG,ATT | M41I | XP_016856482.1 |