Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_007083.4 | 153 | Intron | NP_009014.2 | ||
NM_198041.2 | 153 | Intron | NP_932158.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001317799.1 | 153 | Missense Mutation | TCT,TGT | S27C | NP_001304728.1 |
NM_145207.2 | 153 | Missense Mutation | TCT,TGT | S27C | NP_660208.2 |
XM_005262783.4 | 153 | Missense Mutation | TCT,TGT | S27C | XP_005262840.1 |
XM_011531678.2 | 153 | Missense Mutation | TCT,TGT | S27C | XP_011529980.1 |
XM_011531679.2 | 153 | Missense Mutation | TCT,TGT | S27C | XP_011529981.1 |
XM_017007825.1 | 153 | Missense Mutation | TCT,TGT | S27C | XP_016863314.1 |
XM_017007826.1 | 153 | Missense Mutation | TCT,TGT | S27C | XP_016863315.1 |
XM_017007827.1 | 153 | Missense Mutation | TCT,TGT | S27C | XP_016863316.1 |
XM_017007828.1 | 153 | UTR 5 | XP_016863317.1 | ||
XM_017007829.1 | 153 | Intron | XP_016863318.1 | ||
XM_017007830.1 | 153 | Missense Mutation | TCT,TGT | S27C | XP_016863319.1 |