Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001297763.1 | 318 | Intron | NP_001284692.1 | ||
NM_178544.4 | 318 | Missense Mutation | CCT,CTT | P21L | NP_848639.2 |
XM_011526898.2 | 318 | Intron | XP_011525200.1 | ||
XM_011526899.2 | 318 | Missense Mutation | CCT,CTT | P21L | XP_011525201.1 |