Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001270364.1 | 2860 | Missense Mutation | GCT,GTT | A880V | NP_001257293.1 |
NM_001270365.1 | 2860 | Missense Mutation | GCT,GTT | A769V | NP_001257294.1 |
NM_012190.3 | 2860 | Missense Mutation | GCT,GTT | A870V | NP_036322.2 |
XM_006713481.2 | 2860 | Missense Mutation | GCT,GTT | A870V | XP_006713544.1 |
XM_011512355.1 | 2860 | Missense Mutation | GCT,GTT | A870V | XP_011510657.1 |
XM_017005613.1 | 2860 | Missense Mutation | GCT,GTT | A806V | XP_016861102.1 |
XM_017005614.1 | 2860 | Missense Mutation | GCT,GTT | A796V | XP_016861103.1 |