Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001271807.1 | 600 | Missense Mutation | CCG,CTG | P180L | NP_001258736.1 |
NM_001271808.1 | 600 | Missense Mutation | CCG,CTG | P69L | NP_001258737.1 |
NM_178174.3 | 600 | Missense Mutation | CCG,CTG | P180L | NP_835468.1 |
XM_017010822.1 | 600 | Missense Mutation | CCG,CTG | P239L | XP_016866311.1 |
XM_017010823.1 | 600 | Missense Mutation | CCG,CTG | P180L | XP_016866312.1 |
XM_017010824.1 | 600 | Missense Mutation | CCG,CTG | P180L | XP_016866313.1 |
XM_017010825.1 | 600 | Missense Mutation | CCG,CTG | P239L | XP_016866314.1 |