Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001290223.1 | 5413 | Intron | NP_001277152.1 | ||
NM_001380.4 | 5413 | Intron | NP_001371.1 | ||
XM_011539422.2 | 5413 | Intron | XP_011537724.1 | ||
XM_011539424.1 | 5413 | Intron | XP_011537726.1 | ||
XM_017015813.1 | 5413 | Intron | XP_016871302.1 | ||
XM_017015814.1 | 5413 | Intron | XP_016871303.1 | ||
XM_017015815.1 | 5413 | Intron | XP_016871304.1 | ||
XM_017015816.1 | 5413 | Intron | XP_016871305.1 | ||
XM_017015817.1 | 5413 | Intron | XP_016871306.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001039762.2 | 5413 | Missense Mutation | GAC,GGC | D429G | NP_001034851.1 |
XM_005252694.3 | 5413 | Missense Mutation | GAC,GGC | D429G | XP_005252751.1 |
XM_017016537.1 | 5413 | Missense Mutation | GAC,GGC | D429G | XP_016872026.1 |
XM_017016538.1 | 5413 | Missense Mutation | GAC,GGC | D429G | XP_016872027.1 |
XM_017016539.1 | 5413 | Missense Mutation | GAC,GGC | D429G | XP_016872028.1 |
XM_017016540.1 | 5413 | Missense Mutation | GAC,GGC | D429G | XP_016872029.1 |
XM_017016541.1 | 5413 | Missense Mutation | GAC,GGC | D429G | XP_016872030.1 |
XM_017016542.1 | 5413 | Missense Mutation | GAC,GGC | D429G | XP_016872031.1 |
XM_017016543.1 | 5413 | Intron | XP_016872032.1 |