Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001286974.1 | 2248 | Missense Mutation | CCC,CTC | P699L | NP_001273903.1 |
NM_003798.3 | 2248 | Missense Mutation | CCC,CTC | P699L | NP_003789.1 |
XM_005252291.3 | 2248 | Missense Mutation | CCC,CTC | P699L | XP_005252348.1 |
XM_017015250.1 | 2248 | Missense Mutation | CCC,CTC | P522L | XP_016870739.1 |
XM_017015251.1 | 2248 | Missense Mutation | CCC,CTC | P522L | XP_016870740.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_017832.3 | 2248 | Intron | NP_060302.1 | ||
XM_011518816.2 | 2248 | Intron | XP_011517118.1 |