| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001323316.1 | 2200 | Missense Mutation | CAA,CAC | Q662H | NP_001310245.1 |
| NM_001323317.1 | 2200 | Missense Mutation | CAA,CAC | Q581H | NP_001310246.1 |
| NM_001323318.1 | 2200 | Missense Mutation | CAA,CAC | Q602H | NP_001310247.1 |
| NM_004613.3 | 2200 | Missense Mutation | CAA,CAC | Q662H | NP_004604.2 |
| NM_198951.2 | 2200 | Intron | NP_945189.1 | ||
| XM_011529028.1 | 2200 | Missense Mutation | CAA,CAC | Q662H | XP_011527330.1 |