| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001145102.1 | 347 | Intron | NP_001138574.1 | ||
| NM_001145103.1 | 347 | Intron | NP_001138575.1 | ||
| NM_001145104.1 | 347 | Intron | NP_001138576.1 | ||
| NM_005902.3 | 347 | Missense Mutation | AGC,GGC | S17G | NP_005893.1 |
| XM_011521559.2 | 347 | Missense Mutation | AGC,GGC | S17G | XP_011519861.1 |
| XM_011521560.1 | 347 | Intron | XP_011519862.1 |