Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000354.5 | 1195 | Missense Mutation | CCT,CTT | P383L | NP_000345.2 |
XM_005262180.3 | 1195 | Intron | XP_005262237.1 | ||
XM_006724683.2 | 1195 | Missense Mutation | CCT,CTT | P393L | XP_006724746.1 |