Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001081560.2 | 2442 | Missense Mutation | CCA,CTA | P618L | NP_001075029.1 |
NM_001081562.2 | 2442 | Nonsense Mutation | CAG,TAG | Q617* | NP_001075031.1 |
NM_001081563.2 | 2442 | Missense Mutation | CCA,CTA | P633L | NP_001075032.1 |
NM_001288764.1 | 2442 | Missense Mutation | CCA,CTA | P649L | NP_001275693.1 |
NM_001288765.1 | 2442 | Nonsense Mutation | CAG,TAG | Q533* | NP_001275694.1 |
NM_001288766.1 | 2442 | UTR 3 | NP_001275695.1 | ||
NM_004409.4 | 2442 | Missense Mutation | CCA,CTA | P623L | NP_004400.4 |