| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001193478.1 | 177 | Missense Mutation | CAG,CGG | Q17R | NP_001180407.1 |
| NM_030911.3 | 177 | Missense Mutation | CAG,CGG | Q17R | NP_112173.1 |
| XM_006719871.3 | 177 | Intron | XP_006719934.1 | ||
| XM_011535250.2 | 177 | Intron | XP_011533552.1 | ||
| XM_011535251.1 | 177 | Intron | XP_011533553.1 | ||
| XM_011535253.1 | 177 | UTR 5 | XP_011533555.1 | ||
| XM_017020778.1 | 177 | Intron | XP_016876267.1 | ||
| XM_017020779.1 | 177 | UTR 5 | XP_016876268.1 | ||
| XM_017020780.1 | 177 | UTR 5 | XP_016876269.1 | ||
| XM_017020781.1 | 177 | UTR 5 | XP_016876270.1 | ||
| XM_017020782.1 | 177 | Intron | XP_016876271.1 | ||
| XM_017020783.1 | 177 | UTR 5 | XP_016876272.1 | ||
| XM_017020784.1 | 177 | Intron | XP_016876273.1 |