| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001323627.1 | 1304 | Missense Mutation | GCC,GGC | A442G | NP_001310556.1 |
| NM_013304.2 | 1304 | Missense Mutation | CCG,GCG | P464A | NP_037436.1 |
| XM_005255915.1 | 1304 | UTR 3 | XP_005255972.1 | ||
| XM_006721185.1 | 1304 | Missense Mutation | CCG,GCG | P449A | XP_006721248.1 |
| XM_011523058.1 | 1304 | Missense Mutation | GCC,GGC | A429G | XP_011521360.1 |
| XM_011523059.1 | 1304 | Missense Mutation | CCG,GCG | P411A | XP_011521361.1 |
| XM_011523060.1 | 1304 | Missense Mutation | CCG,GCG | P379A | XP_011521362.1 |