ENST00000357134.10:c.259T>G
MANE Select
|
ENSP00000349654.5:p.Phe87Val
|
|
ENST00000298925.9:c.343T>G
|
ENSP00000298925.5:p.Phe115Val
|
|
ENST00000325319.9:c.259T>G
|
ENSP00000317837.5:p.Phe87Val
|
|
ENST00000357134.9:c.259T>G
|
ENSP00000349654.5:p.Phe87Val
|
|
ENST00000524738.1:n.86T>G
|
|
|
ENST00000527873.5:n.280T>G
|
|
|
ENST00000528046.5:n.442T>G
|
|
|
ENST00000529595.1:n.147T>G
|
|
|
ENST00000532434.5:c.259T>G
|
ENSP00000437170.1:p.Phe87Val
|
|
ENST00000619031.4:c.-454T>G
|
ENSP00000479479.1:n.-454T>G
|
|
NM_001288713.1:c.343T>G
|
NP_001275642.1:p.Phe115Val
|
|
NM_001288714.1:c.259T>G
|
NP_001275643.1:p.Phe87Val
|
|
NM_006157.4:c.259T>G
|
NP_006148.2:p.Phe87Val
|
|
NM_201551.2:c.259T>G
|
NP_963845.1:p.Phe87Val
|
|
NM_006157.5:c.259T>G
MANE Select
|
NP_006148.2:p.Phe87Val
|
|