| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001291484.2 | 659 | Silent Mutation | AAC,AAT | N181N | NP_001278413.1 |
| NM_001308398.1 | 659 | Silent Mutation | AAC,AAT | N181N | NP_001295327.1 |
| NM_004363.5 | 659 | Silent Mutation | AAC,AAT | N181N | NP_004354.3 |
| XM_005258413.3 | 659 | Missense Mutation | AAC,AAT | N181N | XP_005258470.2 |
| XM_011526322.1 | 659 | Missense Mutation | AAC,AAT | N181N | XP_011524624.1 |
| XM_017026145.1 | 659 | Intron | XP_016881634.1 | ||
| XM_017026146.1 | 659 | Intron | XP_016881635.1 |