别名
突变位点
Ref. Build: GRCh37 Ensembl Version: 75
Chr. | Start | Stop | Ref. s | Var. Bases |
16 | 89815152 | 89815152 | G | A |
Transcript | ||||
ENST00000568369.1 |
基因序列
NM_000135.2:c.3263C>003eT
NP_000126.2:p.Ser1088Phe
NC_000016.9:g.89815152G>003eA
ENST00000568369.1:c.3263C>003eT
NP_000126.2:p.Ser1088Phe
NC_000016.9:g.89815152G>003eA
ENST00000568369.1:c.3263C>003eT