Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001014433.2 | 1075 | Missense Mutation | ACC,ATC | T194I | NP_001014433.1 |
NM_001014837.1 | 1075 | Missense Mutation | ACC,ATC | T152I | NP_001014837.1 |
NM_001014838.1 | 1075 | Missense Mutation | ACC,ATC | T152I | NP_001014838.1 |
NM_001014840.1 | 1075 | Missense Mutation | ACC,ATC | T175I | NP_001014840.1 |
NM_015921.2 | 1075 | Missense Mutation | ACC,ATC | T152I | NP_057005.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_002636.4 | 1075 | Intron | NP_002627.1 | ||
NM_024165.2 | 1075 | Intron | NP_077084.1 | ||
XM_011514662.1 | 1075 | Intron | XP_011512964.1 | ||
XM_011514663.1 | 1075 | Intron | XP_011512965.1 | ||
XM_011514664.1 | 1075 | Intron | XP_011512966.1 | ||
XM_011514665.1 | 1075 | Intron | XP_011512967.1 | ||
XM_011514666.1 | 1075 | Intron | XP_011512968.1 | ||
XM_011514669.1 | 1075 | Intron | XP_011512971.1 | ||
XM_011514670.2 | 1075 | Intron | XP_011512972.1 | ||
XM_017010939.1 | 1075 | Intron | XP_016866428.1 |