| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001303058.1 | 652 | Intron | NP_001289987.1 | ||
| NM_001303059.1 | 652 | Missense Mutation | AAC,AGC | N139S | NP_001289988.1 |
| NM_001303060.1 | 652 | Intron | NP_001289989.1 | ||
| NM_001303061.1 | 652 | Missense Mutation | AAC,AGC | N129S | NP_001289990.1 |
| NM_001303062.1 | 652 | Missense Mutation | AAC,AGC | N129S | NP_001289991.1 |
| NM_182547.3 | 652 | Missense Mutation | AAC,AGC | N188S | NP_872353.2 |