Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000106.5 | 949 | Missense Mutation | ATG,GTG | M338V | NP_000097.3 |
NM_001025161.2 | 949 | Missense Mutation | ATG,GTG | M287V | NP_001020332.2 |
XM_011529966.2 | 949 | Intron | XP_011528268.1 | ||
XM_011529968.2 | 949 | Intron | XP_011528270.1 | ||
XM_011529970.2 | 949 | Intron | XP_011528272.1 | ||
XM_011529972.2 | 949 | Intron | XP_011528274.1 |