| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_017742.5 | 1179 | Intron | NP_060212.4 | ||
| XM_006722493.3 | 1179 | Intron | XP_006722556.1 | ||
| XM_011526044.1 | 1179 | Missense Mutation | AAT,AGT | N4S | XP_011524346.1 |
| XM_017025802.1 | 1179 | Intron | XP_016881291.1 |