Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001002000.2 | 712 | Intron | NP_001002000.1 | ||
NM_001002001.2 | 712 | Intron | NP_001002001.1 | ||
NM_001002002.2 | 712 | Intron | NP_001002002.1 | ||
NM_001283021.1 | 712 | Missense Mutation | ATA,ATG | I1M | NP_001269950.1 |
NM_001283022.1 | 712 | Intron | NP_001269951.1 | ||
NM_001283023.1 | 712 | Intron | NP_001269952.1 | ||
NM_016576.4 | 712 | Intron | NP_057660.2 | ||
XM_005267740.3 | 712 | Intron | XP_005267797.1 | ||
XM_005267741.3 | 712 | Intron | XP_005267798.1 | ||
XM_005267742.3 | 712 | Intron | XP_005267799.1 | ||
XM_006720165.2 | 712 | Missense Mutation | ATA,ATG | I1M | XP_006720228.1 |
XM_017021356.1 | 712 | Missense Mutation | ATA,ATG | I1M | XP_016876845.1 |
XM_017021357.1 | 712 | Missense Mutation | ATA,ATG | I1M | XP_016876846.1 |
XM_017021358.1 | 712 | Missense Mutation | ATA,ATG | I1M | XP_016876847.1 |
XM_017021359.1 | 712 | Missense Mutation | ATA,ATG | I1M | XP_016876848.1 |
XM_017021360.1 | 712 | Intron | XP_016876849.1 |