Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005232.4 | 2992 | Missense Mutation | CGC,TGC | R969C | NP_005223.4 |
XM_006715880.3 | 2992 | Missense Mutation | CGC,TGC | R854C | XP_006715943.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001010972.1 | 2992 | Intron | NP_001010972.1 | ||
NM_003461.4 | 2992 | Intron | NP_003452.1 | ||
XM_011516569.2 | 2992 | Intron | XP_011514871.2 | ||
XM_017012587.1 | 2992 | Intron | XP_016868076.1 |