Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001005505.2 | 3374 | Missense Mutation | CCT,CTT | P1135L | NP_001005505.1 |
NM_001174051.2 | 3374 | Missense Mutation | CCT,CTT | P1140L | NP_001167522.1 |
NM_001291101.1 | 3374 | Missense Mutation | CCT,CTT | P1066L | NP_001278030.1 |
NM_006030.3 | 3374 | Missense Mutation | CCT,CTT | P1133L | NP_006021.2 |
XM_005265581.4 | 3374 | Missense Mutation | CCT,CTT | P1134L | XP_005265638.1 |
XM_011534243.2 | 3374 | Missense Mutation | CCT,CTT | P1141L | XP_011532545.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001291284.1 | 3374 | Intron | NP_001278213.1 | ||
NM_007022.4 | 3374 | Intron | NP_008953.1 |