Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001319676.1 | 291 | Missense Mutation | TCT,TTT | S65F | NP_001306605.1 |
NM_006615.2 | 291 | Missense Mutation | TCT,TTT | S65F | NP_006606.1 |
NM_016452.2 | 291 | Missense Mutation | TCT,TTT | S65F | NP_057536.1 |
XM_011544017.1 | 291 | Missense Mutation | TCT,TTT | S65F | XP_011542319.1 |
XM_011544018.1 | 291 | Missense Mutation | TCT,TTT | S65F | XP_011542320.1 |
XM_011544019.2 | 291 | Missense Mutation | TCT,TTT | S65F | XP_011542321.1 |
XM_011544020.1 | 291 | Intron | XP_011542322.1 | ||
XM_017000098.1 | 291 | Missense Mutation | TCT,TTT | S65F | XP_016855587.1 |
XM_017000099.1 | 291 | Intron | XP_016855588.1 |