ENST00000541682.7:c.301T>G
MANE Select
|
ENSP00000446205.2:p.Phe101Val
|
|
ENST00000317814.8:c.286T>G
|
ENSP00000314774.4:p.Phe96Val
|
|
ENST00000541682.6:c.301T>G
|
ENSP00000446205.2:p.Phe101Val
|
|
ENST00000577735.1:c.277T>G
|
ENSP00000462491.1:p.Phe93Val
|
|
NM_001165967.1:c.301T>G
|
NP_001159439.1:p.Phe101Val
|
|
NM_032580.3:c.286T>G
|
NP_115969.2:p.Phe96Val
|
|
XM_011524038.1:c.406T>G
|
XP_011522340.1:p.Phe136Val
|
|
XM_011524039.1:c.397T>G
|
XP_011522341.1:p.Phe133Val
|
|
XM_011524040.1:c.397T>G
|
XP_011522342.1:p.Phe133Val
|
|
XM_011524041.1:c.388T>G
|
XP_011522343.1:p.Phe130Val
|
|
XM_011524042.1:c.259T>G
|
XP_011522344.1:p.Phe87Val
|
|
XR_934203.1:n.69+2149A>C
|
|
|
XM_017025232.1:c.406T>G
|
XP_016880721.1:p.Phe136Val
|
|
XM_024451007.1:c.406T>G
|
XP_024306775.1:p.Phe136Val
|
|
NM_001165967.2:c.301T>G
MANE Select
|
NP_001159439.1:p.Phe101Val
|
|
NM_032580.4:c.286T>G
|
NP_115969.2:p.Phe96Val
|
|