ENST00000320694.13:c.835C>G
|
ENSP00000323512.8:p.Gln279Glu
|
|
ENST00000336483.10:c.925C>G
|
ENSP00000338554.5:p.Gln309Glu
|
|
ENST00000517643.2:c.1735C>G
|
ENSP00000513333.1:p.Gln579Glu
|
|
ENST00000517698.6:c.*705C>G
|
ENSP00000430424.1:n.*705C>G
|
|
ENST00000521657.6:c.1735C>G
|
ENSP00000429277.1:p.Gln579Glu
|
|
ENST00000522084.6:c.925C>G
|
ENSP00000429766.2:p.Gln309Glu
|
|
ENST00000697457.1:c.1660C>G
|
ENSP00000513315.1:p.Gln554Glu
|
|
ENST00000697458.1:c.1735C>G
|
ENSP00000513316.1:p.Gln579Glu
|
|
ENST00000697460.1:c.1210C>G
|
ENSP00000513318.1:p.Gln404Glu
|
|
ENST00000697461.1:c.1735C>G
|
ENSP00000513319.1:p.Gln579Glu
|
|
ENST00000697462.1:c.925C>G
|
ENSP00000513320.1:p.Gln309Glu
|
|
ENST00000697463.1:n.1376C>G
|
|
|
ENST00000697464.1:c.*701C>G
|
ENSP00000513322.1:n.*701C>G
|
|
ENST00000697465.1:c.772C>G
|
ENSP00000513323.1:p.Gln258Glu
|
|
ENST00000697466.1:c.742C>G
|
ENSP00000513324.1:p.Gln248Glu
|
|
ENST00000697467.1:c.646C>G
|
ENSP00000513325.1:p.Gln216Glu
|
|
ENST00000697468.1:c.718C>G
|
ENSP00000513326.1:p.Gln240Glu
|
|
ENST00000697469.1:c.427C>G
|
ENSP00000513327.1:p.Gln143Glu
|
|
ENST00000697470.1:c.331C>G
|
ENSP00000513328.1:p.Gln111Glu
|
|
ENST00000697557.1:c.718C>G
|
ENSP00000513335.1:p.Gln240Glu
|
|
ENST00000521381.6:c.1735C>G
MANE Select
|
ENSP00000428056.1:p.Gln579Glu
|
|
ENST00000320694.12:c.835C>G
|
ENSP00000323512.8:p.Gln279Glu
|
|
ENST00000336483.9:c.925C>G
|
ENSP00000338554.5:p.Gln309Glu
|
|
ENST00000517698.5:c.*705C>G
|
ENSP00000430424.1:n.*705C>G
|
|
ENST00000518813.5:n.2278C>G
|
|
|
ENST00000520550.1:n.1134C>G
|
|
|
ENST00000521381.5:c.1735C>G
|
ENSP00000428056.1:p.Gln579Glu
|
|
ENST00000521657.5:c.1735C>G
|
ENSP00000429277.1:p.Gln579Glu
|
|
ENST00000523872.1:c.646C>G
|
ENSP00000430098.1:p.Gln216Glu
|
|
NM_001242466.1:c.646C>G
|
NP_001229395.1:p.Gln216Glu
|
|
NM_181504.3:c.925C>G
|
NP_852556.2:p.Gln309Glu
|
|
NM_181523.2:c.1735C>G
|
NP_852664.1:p.Gln579Glu
|
|
NM_181524.1:c.835C>G
|
NP_852665.1:p.Gln279Glu
|
|
XM_005248542.2:c.1735C>G
|
XP_005248599.1:p.Gln579Glu
|
|
XM_011543493.1:c.1408C>G
|
XP_011541795.1:p.Gln470Glu
|
|
XM_005248542.3:c.1735C>G
|
XP_005248599.1:p.Gln579Glu
|
|
XM_011543493.3:c.1408C>G
|
XP_011541795.1:p.Gln470Glu
|
|
XM_017009585.2:c.1735C>G
|
XP_016865074.1:p.Gln579Glu
|
|
XM_017009586.1:c.1462C>G
|
XP_016865075.1:p.Gln488Glu
|
|
NM_181523.3:c.1735C>G
MANE Select
|
NP_852664.1:p.Gln579Glu
|
|
NM_001242466.2:c.646C>G
|
NP_001229395.1:p.Gln216Glu
|
|
NM_181504.4:c.925C>G
|
NP_852556.2:p.Gln309Glu
|
|
NM_181524.2:c.835C>G
|
NP_852665.1:p.Gln279Glu
|
|