Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001282566.1 | 228 | Intron | NP_001269495.1 | ||
NM_001282567.1 | 228 | Intron | NP_001269496.1 | ||
NM_001282568.1 | 228 | Missense Mutation | AAT,ACT | N2T | NP_001269497.1 |
NM_001282569.1 | 228 | UTR 5 | NP_001269498.1 | ||
NM_001282570.1 | 228 | Intron | NP_001269499.1 | ||
NM_001282571.1 | 228 | UTR 5 | NP_001269500.1 | ||
NM_001282572.1 | 228 | Missense Mutation | AAT,ACT | N2T | NP_001269501.1 |
NM_001282573.1 | 228 | UTR 5 | NP_001269502.1 | ||
NM_001282574.1 | 228 | Missense Mutation | AAT,ACT | N2T | NP_001269503.1 |
NM_016505.3 | 228 | Missense Mutation | AAT,ACT | N2T | NP_057589.2 |
XM_006710681.3 | 228 | UTR 5 | XP_006710744.1 | ||
XM_011541567.2 | 228 | Missense Mutation | AAT,ACT | N2T | XP_011539869.1 |