Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001252675.1 | 2086 | Missense Mutation | ACC,AGC | T667S | NP_001239604.1 |
NM_001252676.1 | 2086 | Missense Mutation | ACC,AGC | T548S | NP_001239605.1 |
NM_001252677.1 | 2086 | Intron | NP_001239606.1 | ||
NM_032501.3 | 2086 | Missense Mutation | ACC,AGC | T669S | NP_115890.2 |
XM_006723659.1 | 2086 | Missense Mutation | ACC,AGC | T464S | XP_006723722.1 |
XM_011529388.1 | 2086 | Missense Mutation | ACC,AGC | T451S | XP_011527690.1 |