Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_153006.2 | 284 | Missense Mutation | CCT,CTT | P95L | NP_694551.1 |
XM_011524438.1 | 284 | Missense Mutation | CCT,CTT | P95L | XP_011522740.1 |
XM_011524439.2 | 284 | Intron | XP_011522741.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004160.5 | 284 | Intron | NP_004151.3 | ||
XM_011525035.1 | 284 | Intron | XP_011523337.1 |