Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004774.3 | 4815 | Missense Mutation | CCC,CTC | P1557L | NP_004765.2 |
XM_005257465.3 | 4815 | Missense Mutation | CCC,CTC | P1385L | XP_005257522.1 |
XM_006721957.1 | 4815 | Intron | XP_006722020.1 | ||
XM_017024779.1 | 4815 | Missense Mutation | CCC,CTC | P1338L | XP_016880268.1 |