Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001008485.1 | 1527 | Missense Mutation | CTG,GTG | L460V | NP_001008485.1 |
NM_001008486.1 | 1527 | Missense Mutation | CTG,GTG | L424V | NP_001008486.1 |
NM_001008487.1 | 1527 | UTR 3 | NP_001008487.1 | ||
NM_001164475.1 | 1527 | UTR 3 | NP_001157947.1 | ||
NM_017836.3 | 1527 | UTR 3 | NP_060306.3 | ||
XM_005247559.1 | 1527 | Missense Mutation | CTG,GTG | L475V | XP_005247616.1 |
XM_005247562.1 | 1527 | Missense Mutation | CTG,GTG | L460V | XP_005247619.1 |
XM_005247563.2 | 1527 | Missense Mutation | CTG,GTG | L460V | XP_005247620.1 |
XM_005247564.1 | 1527 | UTR 3 | XP_005247621.1 | ||
XM_005247565.2 | 1527 | Missense Mutation | CTG,GTG | L434V | XP_005247622.1 |
XM_006713681.2 | 1527 | Missense Mutation | CTG,GTG | L460V | XP_006713744.1 |
XM_011512945.1 | 1527 | Missense Mutation | CTG,GTG | L449V | XP_011511247.1 |
XM_017006705.1 | 1527 | Missense Mutation | CTG,GTG | L475V | XP_016862194.1 |
XM_017006706.1 | 1527 | UTR 3 | XP_016862195.1 | ||
XM_017006707.1 | 1527 | UTR 3 | XP_016862196.1 | ||
XM_017006708.1 | 1527 | UTR 3 | XP_016862197.1 | ||
XM_017006709.1 | 1527 | UTR 3 | XP_016862198.1 |