Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001171171.1 | 1030 | Missense Mutation | GCT,GTT | A313V | NP_001164642.1 |
NM_001171172.1 | 1030 | Missense Mutation | GCT,GTT | A313V | NP_001164643.1 |
NM_001171174.1 | 1030 | Missense Mutation | GCT,GTT | A345V | NP_001164645.1 |
NM_001337.3 | 1030 | Missense Mutation | GCT,GTT | A313V | NP_001328.1 |