| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001134432.1 | 877 | Intron | NP_001127904.1 | ||
| NM_001134433.1 | 877 | Intron | NP_001127905.1 | ||
| NM_001271650.1 | 877 | Missense Mutation | AAC,GAC | N157D | NP_001258579.1 |
| NM_022461.4 | 877 | Missense Mutation | AAC,GAC | N269D | NP_071906.1 |
| XM_005265392.2 | 877 | Missense Mutation | AAC,GAC | N269D | XP_005265449.1 |
| XM_011534009.2 | 877 | Missense Mutation | AAC,GAC | N272D | XP_011532311.1 |
| XM_011534010.2 | 877 | Intron | XP_011532312.1 | ||
| XM_011534011.2 | 877 | Intron | XP_011532313.1 |