Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001167911.1 | 2412 | Missense Mutation | CCC,CTC | P740L | NP_001161383.1 |
NM_001167912.1 | 2412 | Missense Mutation | CCC,CTC | P785L | NP_001161384.1 |
NM_001167915.1 | 2412 | Intron | NP_001161387.1 | ||
NM_001167916.1 | 2412 | Intron | NP_001161388.1 | ||
NM_001167917.1 | 2412 | Intron | NP_001161389.1 | ||
NM_024621.2 | 2412 | Missense Mutation | CCC,CTC | P785L | NP_078897.2 |
XM_011513134.2 | 2412 | Missense Mutation | CCC,CTC | P796L | XP_011511436.1 |
XM_011513135.1 | 2412 | Missense Mutation | CCC,CTC | P740L | XP_011511437.1 |