Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001009996.2 | 1206 | Missense Mutation | TGC,TTC | C277F | NP_001009996.1 |
NM_001276405.1 | 1206 | Missense Mutation | TGC,TTC | C277F | NP_001263334.1 |
NM_018114.5 | 1206 | Missense Mutation | TGC,TTC | C110F | NP_060584.3 |
XM_005265269.3 | 1206 | Missense Mutation | TGC,TTC | C277F | XP_005265326.1 |
XM_006713219.2 | 1206 | Missense Mutation | TGC,TTC | C110F | XP_006713282.1 |
XM_011533891.1 | 1206 | Missense Mutation | TGC,TTC | C277F | XP_011532193.1 |
XM_011533892.1 | 1206 | Missense Mutation | TGC,TTC | C110F | XP_011532194.1 |
XM_011533893.1 | 1206 | Missense Mutation | TGC,TTC | C277F | XP_011532195.1 |
XM_017006723.1 | 1206 | Missense Mutation | TGC,TTC | C110F | XP_016862212.1 |