| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_018477.2 | 201 | Missense Mutation | ATG,CTG | M48L | NP_060947.1 |
| XM_011536960.1 | 201 | Missense Mutation | ATG,CTG | M48L | XP_011535262.1 |
| XM_011536961.1 | 201 | Missense Mutation | ATG,CTG | M48L | XP_011535263.1 |
| XM_011536962.2 | 201 | UTR 5 | XP_011535264.1 | ||
| XM_011536963.2 | 201 | UTR 5 | XP_011535265.1 |