| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001288998.1 | 2927 | Missense Mutation | CCG,CTG | P930L | NP_001275927.1 |
| NM_001288999.1 | 2927 | Missense Mutation | CCG,CTG | P933L | NP_001275928.1 |
| NM_016573.3 | 2927 | Missense Mutation | CCG,CTG | P959L | NP_057657.2 |
| XM_005259927.2 | 2927 | Missense Mutation | CCG,CTG | P956L | XP_005259984.1 |
| XM_011528048.2 | 2927 | Missense Mutation | CCG,CTG | P838L | XP_011526350.1 |
| XM_017026861.1 | 2927 | UTR 3 | XP_016882350.1 | ||
| XM_017026862.1 | 2927 | Intron | XP_016882351.1 |