Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_002446.3 | 1001 | Missense Mutation | AAC,ACC | N238T | NP_002437.2 |
XM_006723222.2 | 1001 | UTR 5 | XP_006723285.1 | ||
XM_006723223.3 | 1001 | Intron | XP_006723286.1 | ||
XM_011526981.2 | 1001 | Missense Mutation | AAC,ACC | N238T | XP_011525283.1 |
XM_011526982.2 | 1001 | Missense Mutation | AAC,ACC | N238T | XP_011525284.1 |