Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001177996.1 | 1029 | Missense Mutation | TCG,TTG | S226L | NP_001171467.1 |
NM_001177997.1 | 1029 | Missense Mutation | TCG,TTG | S213L | NP_001171468.1 |
NM_144671.4 | 1029 | Missense Mutation | TCG,TTG | S213L | NP_653272.2 |
XM_006719257.3 | 1029 | Missense Mutation | TCG,TTG | S213L | XP_006719320.1 |
XM_011537976.2 | 1029 | Missense Mutation | TCG,TTG | S213L | XP_011536278.1 |
XM_017018883.1 | 1029 | Missense Mutation | TCG,TTG | S213L | XP_016874372.1 |