| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001320308.1 | 117 | Missense Mutation | GCC,GGC | A31G | NP_001307237.1 |
| NM_178868.4 | 117 | Missense Mutation | GCC,GGC | A31G | NP_849199.2 |
| XM_011533416.2 | 117 | Missense Mutation | GCC,GGC | A31G | XP_011531718.1 |
| XM_017005779.1 | 117 | Intron | XP_016861268.1 | ||
| XM_017005780.1 | 117 | Intron | XP_016861269.1 |