Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004295.3 | 340 | Missense Mutation | CCG,CTG | P70L | NP_004286.2 |
XM_011525504.2 | 340 | Missense Mutation | CCG,CTG | P77L | XP_011523806.1 |
XM_011525505.2 | 340 | Missense Mutation | CCG,CTG | P61L | XP_011523807.1 |
XM_011525506.2 | 340 | Missense Mutation | CCG,CTG | P54L | XP_011523808.1 |
XM_011525507.2 | 340 | UTR 5 | XP_011523809.1 | ||
XM_011525508.2 | 340 | UTR 5 | XP_011523810.1 |