| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001316887.1 | 770 | Missense Mutation | AAT,GAT | N162D | NP_001303816.1 |
| NM_001316888.1 | 770 | Missense Mutation | AAT,GAT | N162D | NP_001303817.1 |
| NM_001316889.1 | 770 | Missense Mutation | AAT,GAT | N162D | NP_001303818.1 |
| NM_021796.3 | 770 | Missense Mutation | AAT,GAT | N162D | NP_068568.1 |
| XM_011531257.2 | 770 | Missense Mutation | AAT,GAT | N162D | XP_011529559.1 |
| XM_011531260.2 | 770 | Missense Mutation | AAT,GAT | N162D | XP_011529562.1 |
| XM_017029236.1 | 770 | Missense Mutation | AAT,GAT | N162D | XP_016884725.1 |