Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001007122.3 | 2315 | Missense Mutation | CCA,CTA | P711L | NP_001007123.1 |
NM_001281805.1 | 2315 | Missense Mutation | CCA,CTA | P666L | NP_001268734.1 |
NM_001281806.1 | 2315 | Missense Mutation | CCA,CTA | P666L | NP_001268735.1 |
XM_005272425.4 | 2315 | Missense Mutation | CCA,CTA | P711L | XP_005272482.1 |
XM_011521235.2 | 2315 | Missense Mutation | CCA,CTA | P634L | XP_011519537.1 |
XM_017021924.1 | 2315 | Intron | XP_016877413.1 |