Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_024068.3 | 736 | Missense Mutation | CCT,GCT | P198A | NP_076973.1 |
XM_005269146.2 | 736 | Missense Mutation | CCT,GCT | P241A | XP_005269203.1 |
XM_005269147.2 | 736 | Missense Mutation | CCT,GCT | P214A | XP_005269204.1 |
XM_005269148.4 | 736 | Missense Mutation | CCT,GCT | P198A | XP_005269205.1 |
XM_005269149.4 | 736 | Missense Mutation | CCT,GCT | P198A | XP_005269206.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001135195.1 | 736 | Intron | NP_001128667.1 | ||
NM_173596.2 | 736 | Intron | NP_775867.2 | ||
XM_005268803.1 | 736 | Intron | XP_005268860.1 | ||
XM_011538198.1 | 736 | Intron | XP_011536500.1 | ||
XM_011538199.1 | 736 | Intron | XP_011536501.1 | ||
XM_011538200.1 | 736 | Intron | XP_011536502.1 | ||
XM_011538201.1 | 736 | Intron | XP_011536503.1 | ||
XM_017019185.1 | 736 | Intron | XP_016874674.1 | ||
XM_017019186.1 | 736 | Intron | XP_016874675.1 | ||
XM_017019187.1 | 736 | Intron | XP_016874676.1 |