Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_021026.2 | 3914 | Intron | NP_066306.2 | ||
XM_011530298.2 | 3914 | Missense Mutation | ACG,ATG | T98M | XP_011528600.1 |
XM_011530299.2 | 3914 | Intron | XP_011528601.1 | ||
XM_017028900.1 | 3914 | Missense Mutation | ACG,ATG | T98M | XP_016884389.1 |
XM_017028901.1 | 3914 | Missense Mutation | ACG,ATG | T98M | XP_016884390.1 |
XM_017028902.1 | 3914 | Missense Mutation | ACG,ATG | T98M | XP_016884391.1 |