| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001284377.1 | 470 | Intron | NP_001271306.1 | ||
| NM_001284378.1 | 470 | Intron | NP_001271307.1 | ||
| NM_001284379.1 | 470 | Intron | NP_001271308.1 | ||
| NM_001321844.1 | 470 | Missense Mutation | GAT,GGT | D109G | NP_001308773.1 |
| NM_001321845.1 | 470 | Missense Mutation | GAT,GGT | D87G | NP_001308774.1 |
| NM_001321846.1 | 470 | Intron | NP_001308775.1 | ||
| NM_001321847.1 | 470 | Missense Mutation | GAT,GGT | D111G | NP_001308776.1 |
| NM_001321848.1 | 470 | Missense Mutation | GAT,GGT | D139G | NP_001308777.1 |
| NM_017828.4 | 470 | Missense Mutation | GAT,GGT | D133G | NP_060298.2 |
| XM_005254509.3 | 470 | Missense Mutation | GAT,GGT | D160G | XP_005254566.1 |
| XM_005254510.3 | 470 | Missense Mutation | GAT,GGT | D138G | XP_005254567.1 |
| XM_011521739.1 | 470 | Missense Mutation | GAT,GGT | D163G | XP_011520041.1 |
| XM_011521740.1 | 470 | Missense Mutation | GAT,GGT | D141G | XP_011520042.1 |
| XM_011521741.1 | 470 | Intron | XP_011520043.1 | ||
| XM_017022385.1 | 470 | Intron | XP_016877874.1 |