Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001025579.2 | 406 | Missense Mutation | CCA,CTA | P7L | NP_001020750.1 |
NM_030808.4 | 406 | Missense Mutation | CCA,CTA | P7L | NP_110435.1 |
XM_011524013.1 | 406 | Missense Mutation | CCA,CTA | P7L | XP_011522315.1 |
XM_017025183.1 | 406 | Missense Mutation | CCA,CTA | P20L | XP_016880672.1 |
XM_017025184.1 | 406 | Missense Mutation | CCA,CTA | P20L | XP_016880673.1 |
XM_017025185.1 | 406 | Missense Mutation | CCA,CTA | P7L | XP_016880674.1 |
XM_017025186.1 | 406 | Missense Mutation | CCA,CTA | P20L | XP_016880675.1 |
XM_017025187.1 | 406 | Missense Mutation | CCA,CTA | P7L | XP_016880676.1 |
XM_017025188.1 | 406 | Missense Mutation | CCA,CTA | P20L | XP_016880677.1 |