| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001039886.3 | 1519 | Intron | NP_001034975.2 | ||
| NM_001321424.1 | 1519 | Intron | NP_001308353.1 | ||
| NM_001321425.1 | 1519 | Intron | NP_001308354.1 | ||
| XM_005258909.3 | 1519 | Missense Mutation | CAC,CGC | H425R | XP_005258966.1 |