| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001009877.2 | 1599 | Silent Mutation | CAC,CAT | H482H | NP_001009877.2 |
| NM_001317951.1 | 1599 | Silent Mutation | CAC,CAT | H439H | NP_001304880.1 |
| NM_023924.4 | 1599 | Silent Mutation | CAC,CAT | H535H | NP_076413.3 |
| XM_006714494.3 | 1599 | Intron | XP_006714557.1 | ||
| XM_017009780.1 | 1599 | Intron | XP_016865269.1 |