Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_024556.3 | 941 | Missense Mutation | ACG,ATG | T276M | NP_078832.1 |
XM_005271665.3 | 941 | Missense Mutation | ACG,ATG | T276M | XP_005271722.1 |
XM_011542977.2 | 941 | Missense Mutation | ACG,ATG | T276M | XP_011541279.1 |
XM_011542978.2 | 941 | Missense Mutation | ACG,ATG | T121M | XP_011541280.1 |
XM_017018285.1 | 941 | Missense Mutation | ACG,ATG | T276M | XP_016873774.1 |
XM_017018286.1 | 941 | Missense Mutation | ACG,ATG | T121M | XP_016873775.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001177842.1 | 941 | Intron | NP_001171313.1 | ||
NM_003139.3 | 941 | Intron | NP_003130.2 | ||
XM_017018179.1 | 941 | UTR 3 | XP_016873668.1 |