Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001012267.2 | 757 | Missense Mutation | ACG,ATG | T72M | NP_001012267.1 |
NM_001286969.1 | 757 | Intron | NP_001273898.1 | ||
NM_001286971.1 | 757 | Intron | NP_001273900.1 | ||
XM_011518685.2 | 757 | Missense Mutation | ACG,ATG | T72M | XP_011516987.1 |
XM_011518689.1 | 757 | Missense Mutation | ACG,ATG | T72M | XP_011516991.1 |
XM_017014715.1 | 757 | Missense Mutation | ACG,ATG | T72M | XP_016870204.1 |