| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001171156.1 | 1775 | Missense Mutation | AAC,AGC | N613S | NP_001164627.1 |
| NM_001171157.1 | 1775 | Intron | NP_001164628.1 | ||
| NM_001171158.1 | 1775 | Missense Mutation | AAC,AGC | N528S | NP_001164629.1 |
| NM_001171159.1 | 1775 | Missense Mutation | AAC,AGC | N518S | NP_001164630.1 |
| NM_001171161.1 | 1775 | Missense Mutation | AAC,AGC | N428S | NP_001164632.1 |
| NM_001322105.1 | 1775 | Missense Mutation | AAC,AGC | N486S | NP_001309034.1 |
| NM_033130.4 | 1775 | Missense Mutation | AAC,AGC | N671S | NP_149121.2 |
| XM_005259366.4 | 1775 | Missense Mutation | AAC,AGC | N581S | XP_005259423.1 |
| XM_005259367.3 | 1775 | Missense Mutation | AAC,AGC | N523S | XP_005259424.1 |
| XM_011527439.1 | 1775 | Missense Mutation | AAC,AGC | N623S | XP_011525741.1 |