| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001032292.2 | 1113 | Missense Mutation | CCG,TCG | P100S | NP_001027463.1 |
| NM_003450.2 | 1113 | Missense Mutation | CCG,TCG | P100S | NP_003441.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001284527.1 | 1113 | Intron | NP_001271456.1 | ||
| NM_001284528.1 | 1113 | Intron | NP_001271457.1 | ||
| NM_001284529.1 | 1113 | Intron | NP_001271458.1 | ||
| NM_001324340.1 | 1113 | Intron | NP_001311269.1 | ||
| NM_001324341.1 | 1113 | Intron | NP_001311270.1 | ||
| NM_001324342.1 | 1113 | Intron | NP_001311271.1 | ||
| NM_001324343.1 | 1113 | Intron | NP_001311272.1 | ||
| NM_001324344.1 | 1113 | Intron | NP_001311273.1 | ||
| NM_001324345.1 | 1113 | Intron | NP_001311274.1 | ||
| NM_001324346.1 | 1113 | Intron | NP_001311275.1 | ||
| NM_017810.3 | 1113 | Intron | NP_060280.2 |