ENST00000380044.6:c.334A>C
MANE Select
|
ENSP00000369383.1:p.Asn112His
|
|
ENST00000233545.6:c.334A>C
|
ENSP00000233545.2:p.Asn112His
|
|
ENST00000357186.10:c.166A>C
|
ENSP00000349713.6:p.Asn56His
|
|
ENST00000380044.5:c.334A>C
|
ENSP00000369383.1:p.Asn112His
|
|
ENST00000402310.5:c.334A>C
|
ENSP00000383955.1:p.Asn112His
|
|
ENST00000402722.5:c.299A>C
|
ENSP00000386000.1:p.Ter100Ser
|
|
ENST00000403262.6:c.334A>C
|
ENSP00000385671.1:p.Asn112His
|
|
ENST00000405076.5:c.187-289A>C
|
ENSP00000385175.1:n.187-289A>C
|
|
ENST00000405983.5:c.379A>C
|
ENSP00000384586.1:p.Asn127His
|
|
ENST00000415514.5:c.*135A>C
|
ENSP00000388043.1:n.*135A>C
|
|
ENST00000426513.6:c.299A>C
|
ENSP00000403824.2:p.Ter100Ser
|
|
ENST00000428910.5:c.256A>C
|
ENSP00000405235.1:p.Asn86His
|
|
ENST00000430991.5:c.209+145A>C
|
|
|
ENST00000475085.1:n.362A>C
|
|
|
ENST00000616446.1:n.311A>C
|
|
|
ENST00000616707.1:n.853A>C
|
|
|
ENST00000617583.4:n.360A>C
|
|
|
ENST00000621183.4:n.390A>C
|
|
|
ENST00000621470.4:n.350A>C
|
|
|
ENST00000622003.4:n.507A>C
|
|
|
NM_002437.4:c.334A>C
|
NP_002428.1:p.Asn112His
|
|
XM_005264326.2:c.334A>C
|
XP_005264383.1:p.Asn112His
|
|
XM_005264327.2:c.175A>C
|
XP_005264384.1:p.Asn59His
|
|
XM_006712021.2:c.286A>C
|
XP_006712084.1:p.Asn96His
|
|
XM_005264326.4:c.334A>C
|
XP_005264383.1:p.Asn112His
|
|
XM_006712021.3:c.286A>C
|
XP_006712084.1:p.Asn96His
|
|
XM_017004150.1:c.316A>C
|
XP_016859639.1:p.Asn106His
|
|
XM_017004151.1:c.286A>C
|
XP_016859640.1:p.Asn96His
|
|
XM_017004152.1:c.175A>C
|
XP_016859641.1:p.Asn59His
|
|
XM_024452913.1:c.286A>C
|
XP_024308681.1:p.Asn96His
|
|
NM_002437.5:c.334A>C
MANE Select
|
NP_002428.1:p.Asn112His
|
|