Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001184935.1 | 1067 | Missense Mutation | ATG,CTG | M527L | NP_001171864.1 |
NM_004883.2 | 1067 | Missense Mutation | ATG,CTG | M593L | NP_004874.1 |
NM_013981.3 | 1067 | Missense Mutation | ATG,CTG | M587L | NP_053584.1 |
NM_013982.2 | 1067 | Missense Mutation | ATG,CTG | M601L | NP_053585.1 |
NM_013983.2 | 1067 | Missense Mutation | ATG,CTG | M595L | NP_053586.1 |
XM_005268533.3 | 1067 | Missense Mutation | ATG,CTG | M202L | XP_005268590.1 |
XM_006714810.3 | 1067 | Intron | XP_006714873.1 | ||
XM_011537713.2 | 1067 | Intron | XP_011536015.1 | ||
XM_017010064.1 | 1067 | Missense Mutation | ATG,CTG | M213L | XP_016865553.1 |
XM_017010065.1 | 1067 | Missense Mutation | ATG,CTG | M210L | XP_016865554.1 |
XM_017010066.1 | 1067 | Intron | XP_016865555.1 |