ENST00000554809.6:c.70C>A
|
ENSP00000450632.2:p.His24Asn
|
|
ENST00000556036.6:c.1858C>A
|
ENSP00000450596.1:p.His620Asn
|
|
ENST00000556250.6:c.1651C>A
|
ENSP00000452033.2:p.His551Asn
|
|
ENST00000696641.1:c.1699C>A
|
ENSP00000512774.1:p.His567Asn
|
|
ENST00000696642.1:c.*669C>A
|
ENSP00000512775.1:n.*669C>A
|
|
ENST00000696646.1:c.*669C>A
|
ENSP00000512777.1:n.*669C>A
|
|
ENST00000696647.1:c.1858C>A
|
ENSP00000512778.1:p.His620Asn
|
|
ENST00000696648.1:c.1858C>A
|
ENSP00000512779.1:p.His620Asn
|
|
ENST00000696649.1:c.1858C>A
|
ENSP00000512780.1:p.His620Asn
|
|
ENST00000696650.1:n.1806C>A
|
|
|
ENST00000696658.1:n.2408C>A
|
|
|
ENST00000696662.1:c.1780C>A
|
ENSP00000512788.1:p.His594Asn
|
|
ENST00000696663.1:c.675C>A
|
|
|
ENST00000696664.1:c.675C>A
|
|
|
ENST00000696675.1:c.1858C>A
|
ENSP00000512799.1:p.His620Asn
|
|
ENST00000696683.1:c.675C>A
|
|
|
ENST00000696684.1:c.675C>A
|
|
|
ENST00000696685.1:c.675C>A
|
|
|
ENST00000267430.10:c.1858C>A
MANE Select
|
ENSP00000267430.5:p.His620Asn
|
|
ENST00000267430.9:c.1858C>A
|
ENSP00000267430.5:p.His620Asn
|
|
ENST00000542564.6:c.1780C>A
|
ENSP00000442493.2:p.His594Asn
|
|
ENST00000556036.5:c.1858C>A
|
ENSP00000450596.1:p.His620Asn
|
|
ENST00000556250.5:c.406C>A
|
ENSP00000452033.1:p.His136Asn
|
|
NM_001308133.1:c.1780C>A
|
NP_001295062.1:p.His594Asn
|
|
NM_001308134.1:c.1858C>A
|
NP_001295063.1:p.His620Asn
|
|
NM_020937.2:c.1858C>A , LRG_502t1:c.1858C>A
|
NP_065988.1:p.His620Asn
|
|
NM_020937.3:c.1858C>A
|
NP_065988.1:p.His620Asn
|
|
XM_011537034.1:c.1858C>A
|
XP_011535336.1:p.His620Asn
|
|
XM_011537035.1:c.1780C>A
|
XP_011535337.1:p.His594Asn
|
|
XM_011537036.1:c.1858C>A
|
XP_011535338.1:p.His620Asn
|
|
XM_011537034.2:c.1858C>A
|
XP_011535336.1:p.His620Asn
|
|
XM_011537035.3:c.1780C>A
|
XP_011535337.1:p.His594Asn
|
|
XM_017021523.1:c.1858C>A
|
XP_016877012.1:p.His620Asn
|
|
XM_017021524.2:c.895C>A
|
XP_016877013.1:p.His299Asn
|
|
XM_017021525.2:c.673C>A
|
XP_016877014.1:p.His225Asn
|
|
XM_017021526.2:c.673C>A
|
XP_016877015.1:p.His225Asn
|
|
XM_017021527.1:c.673C>A
|
XP_016877016.1:p.His225Asn
|
|
XR_001750470.1:n.1950C>A
|
|
|
XR_001750471.2:n.1950C>A
|
|
|
XR_001750472.1:n.1950C>A
|
|
|
NM_020937.4:c.1858C>A
MANE Select
|
NP_065988.1:p.His620Asn
|
|
NM_001308133.2:c.1780C>A
|
NP_001295062.1:p.His594Asn
|
|
NM_001308134.2:c.1858C>A
|
NP_001295063.1:p.His620Asn
|
|