Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001067.3 | 4456 | Missense Mutation | TCT,TTT | S1452F | NP_001058.2 |
XM_005257632.1 | 4456 | Missense Mutation | TCT,TTT | S1440F | XP_005257689.1 |
XM_011525165.1 | 4456 | Intron | XP_011523467.1 |