| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001321150.1 | 520 | Intron | NP_001308079.1 | ||
| NM_003367.3 | 520 | Missense Mutation | CAA,CGA | Q166R | NP_003358.1 |
| NM_207291.2 | 520 | Missense Mutation | CAA,CGA | Q99R | NP_997174.1 |
| XM_005259197.3 | 520 | Missense Mutation | CAA,CGA | Q166R | XP_005259254.1 |
| XM_011527260.2 | 520 | Missense Mutation | CAA,CGA | Q166R | XP_011525562.1 |
| XM_011527261.2 | 520 | Missense Mutation | CAA,CGA | Q166R | XP_011525563.1 |
| XM_017027199.1 | 520 | Missense Mutation | CAA,CGA | Q99R | XP_016882688.1 |