| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001040002.1 | 971 | Missense Mutation | CAA,CGA | Q69R | NP_001035091.1 |
| NM_004527.3 | 971 | Missense Mutation | CAA,CGA | Q184R | NP_004518.1 |
| NM_013999.3 | 971 | Intron | NP_054705.1 | ||
| XM_011524818.1 | 971 | Missense Mutation | CAA,CGA | Q184R | XP_011523120.1 |