Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001032287.2 | 1514 | Intron | NP_001027458.1 | ||
NM_001127362.1 | 1514 | Intron | NP_001120834.1 | ||
NM_003297.3 | 1514 | Missense Mutation | CAG,CTG | Q520L | NP_003288.2 |
XM_005269133.2 | 1514 | Missense Mutation | CAG,CTG | Q515L | XP_005269190.1 |
XM_006719584.2 | 1514 | Missense Mutation | CAG,CTG | Q474L | XP_006719647.1 |
XM_006719585.2 | 1514 | Missense Mutation | CAG,CTG | Q343L | XP_006719648.1 |
XM_011538716.2 | 1514 | Intron | XP_011537018.1 | ||
XM_011538717.2 | 1514 | Missense Mutation | CAG,CTG | Q424L | XP_011537019.1 |