Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001193509.1 | 349 | Intron | NP_001180438.1 | ||
NM_017735.4 | 349 | Missense Mutation | GTC,TTC | V26F | NP_060205.3 |
XM_005264416.1 | 349 | Missense Mutation | GTC,TTC | V26F | XP_005264473.1 |
XM_011532958.1 | 349 | Missense Mutation | GTC,TTC | V26F | XP_011531260.1 |