Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001277339.1 | 4325 | Intron | NP_001264268.1 | ||
XM_017010153.1 | 4325 | Missense Mutation | TCG,TTG | S102L | XP_016865642.1 |
XM_017010154.1 | 4325 | Missense Mutation | TCG,TTG | S102L | XP_016865643.1 |