Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005668.5 | 1360 | Missense Mutation | AAT,CAT | N344H | NP_005659.1 |
NM_175052.2 | 1360 | Intron | NP_778222.1 | ||
XM_005272078.2 | 1360 | Intron | XP_005272135.1 | ||
XM_011543630.1 | 1360 | Missense Mutation | AAT,CAT | N246H | XP_011541932.1 |