ENST00000554809.6:c.10C>G
|
ENSP00000450632.2:p.Gln4Glu
|
|
ENST00000556036.6:c.1798C>G
|
ENSP00000450596.1:p.Gln600Glu
|
|
ENST00000556250.6:c.1591C>G
|
ENSP00000452033.2:p.Gln531Glu
|
|
ENST00000696641.1:c.1639C>G
|
ENSP00000512774.1:p.Gln547Glu
|
|
ENST00000696642.1:c.*609C>G
|
ENSP00000512775.1:n.*609C>G
|
|
ENST00000696646.1:c.*609C>G
|
ENSP00000512777.1:n.*609C>G
|
|
ENST00000696647.1:c.1798C>G
|
ENSP00000512778.1:p.Gln600Glu
|
|
ENST00000696648.1:c.1798C>G
|
ENSP00000512779.1:p.Gln600Glu
|
|
ENST00000696649.1:c.1798C>G
|
ENSP00000512780.1:p.Gln600Glu
|
|
ENST00000696650.1:n.1746C>G
|
|
|
ENST00000696658.1:n.2348C>G
|
|
|
ENST00000696662.1:c.1720C>G
|
ENSP00000512788.1:p.Gln574Glu
|
|
ENST00000696663.1:c.615C>G
|
|
|
ENST00000696664.1:c.615C>G
|
|
|
ENST00000696675.1:c.1798C>G
|
ENSP00000512799.1:p.Gln600Glu
|
|
ENST00000696683.1:c.615C>G
|
|
|
ENST00000696684.1:c.615C>G
|
|
|
ENST00000696685.1:c.615C>G
|
|
|
ENST00000267430.10:c.1798C>G
MANE Select
|
ENSP00000267430.5:p.Gln600Glu
|
|
ENST00000267430.9:c.1798C>G
|
ENSP00000267430.5:p.Gln600Glu
|
|
ENST00000542564.6:c.1720C>G
|
ENSP00000442493.2:p.Gln574Glu
|
|
ENST00000556036.5:c.1798C>G
|
ENSP00000450596.1:p.Gln600Glu
|
|
ENST00000556250.5:c.346C>G
|
ENSP00000452033.1:p.Gln116Glu
|
|
NM_001308133.1:c.1720C>G
|
NP_001295062.1:p.Gln574Glu
|
|
NM_001308134.1:c.1798C>G
|
NP_001295063.1:p.Gln600Glu
|
|
NM_020937.2:c.1798C>G , LRG_502t1:c.1798C>G
|
NP_065988.1:p.Gln600Glu
|
|
NM_020937.3:c.1798C>G
|
NP_065988.1:p.Gln600Glu
|
|
XM_011537034.1:c.1798C>G
|
XP_011535336.1:p.Gln600Glu
|
|
XM_011537035.1:c.1720C>G
|
XP_011535337.1:p.Gln574Glu
|
|
XM_011537036.1:c.1798C>G
|
XP_011535338.1:p.Gln600Glu
|
|
XM_011537034.2:c.1798C>G
|
XP_011535336.1:p.Gln600Glu
|
|
XM_011537035.3:c.1720C>G
|
XP_011535337.1:p.Gln574Glu
|
|
XM_017021523.1:c.1798C>G
|
XP_016877012.1:p.Gln600Glu
|
|
XM_017021524.2:c.835C>G
|
XP_016877013.1:p.Gln279Glu
|
|
XM_017021525.2:c.613C>G
|
XP_016877014.1:p.Gln205Glu
|
|
XM_017021526.2:c.613C>G
|
XP_016877015.1:p.Gln205Glu
|
|
XM_017021527.1:c.613C>G
|
XP_016877016.1:p.Gln205Glu
|
|
XR_001750470.1:n.1890C>G
|
|
|
XR_001750471.2:n.1890C>G
|
|
|
XR_001750472.1:n.1890C>G
|
|
|
NM_020937.4:c.1798C>G
MANE Select
|
NP_065988.1:p.Gln600Glu
|
|
NM_001308133.2:c.1720C>G
|
NP_001295062.1:p.Gln574Glu
|
|
NM_001308134.2:c.1798C>G
|
NP_001295063.1:p.Gln600Glu
|
|