Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001278926.1 | 218 | Missense Mutation | GCT,TCT | A7S | NP_001265855.1 |
NM_001278927.1 | 218 | UTR 5 | NP_001265856.1 | ||
NM_001278929.1 | 218 | UTR 5 | NP_001265858.1 | ||
NM_015342.3 | 218 | Missense Mutation | CGC,CTC | R49L | NP_056157.1 |
XM_005248474.3 | 218 | Missense Mutation | GCT,TCT | A7S | XP_005248531.1 |
XM_006714583.3 | 218 | UTR 5 | XP_006714646.1 | ||
XM_011543295.1 | 218 | Intron | XP_011541597.1 | ||
XM_017009286.1 | 218 | Intron | XP_016864775.1 |