ENST00000350026.11:c.3788A>G
|
ENSP00000055163.8:p.Gln1263Arg
|
|
ENST00000414678.8:c.3857A>G
|
ENSP00000412835.3:p.Gln1286Arg
|
|
ENST00000637015.2:c.4076A>G
|
ENSP00000489729.2:p.Gln1359Arg
|
|
ENST00000346085.10:c.3827A>G
|
ENSP00000344546.5:p.Gln1276Arg
|
|
ENST00000350026.10:c.3539A>G
|
ENSP00000055163.7:p.Gln1180Arg
|
|
ENST00000414678.7:c.2105A>G
|
ENSP00000412835.2:p.Gln702Arg
|
|
ENST00000635849.1:c.1268A>G
|
ENSP00000490948.1:p.Gln423Arg
|
|
ENST00000635957.1:c.902A>G
|
ENSP00000490385.1:p.Gln301Arg
|
|
ENST00000636930.2:c.3947A>G
MANE Select
|
ENSP00000490491.2:p.Gln1316Arg
|
|
ENST00000636940.1:n.1944A>G
|
|
|
ENST00000637015.1:c.1315A>G
|
|
|
ENST00000637568.1:c.1229A>G
|
|
|
ENST00000637741.1:n.613A>G
|
|
|
ENST00000637810.1:c.1289A>G
|
ENSP00000489636.1:p.Gln430Arg
|
|
ENST00000637904.1:c.1448A>G
|
ENSP00000490550.1:p.Gln483Arg
|
|
ENST00000647938.1:c.3578A>G
|
ENSP00000498155.1:p.Gln1193Arg
|
|
ENST00000346085.9:c.3578A>G
|
ENSP00000344546.4:p.Gln1193Arg
|
|
ENST00000350026.9:c.3539A>G
|
ENSP00000055163.7:p.Gln1180Arg
|
|
ENST00000414678.6:c.2105A>G
|
ENSP00000412835.2:p.Gln702Arg
|
|
NM_017519.2:c.3539A>G
|
NP_059989.2:p.Gln1180Arg
|
|
NM_020732.3:c.3578A>G
|
NP_065783.3:p.Gln1193Arg
|
|
XM_005267069.3:c.3698A>G
|
XP_005267126.2:p.Gln1233Arg
|
|
XM_011535984.1:c.2777A>G
|
XP_011534286.1:p.Gln926Arg
|
|
XM_011535985.1:c.2597A>G
|
XP_011534287.1:p.Gln866Arg
|
|
XM_011535986.1:c.2357A>G
|
XP_011534288.1:p.Gln786Arg
|
|
XM_011535987.1:c.1976A>G
|
XP_011534289.1:p.Gln659Arg
|
|
XM_011535988.1:c.839A>G
|
XP_011534290.1:p.Gln280Arg
|
|
NM_001346813.1:c.3698A>G
|
NP_001333742.1:p.Gln1233Arg
|
|
NM_001363725.1:c.1448A>G
|
NP_001350654.1:p.Gln483Arg
|
|
XM_011535984.2:c.3908A>G
|
XP_011534286.2:p.Gln1303Arg
|
|
XM_011535988.3:c.839A>G
|
XP_011534290.1:p.Gln280Arg
|
|
XM_017011103.2:c.3809A>G
|
XP_016866592.1:p.Gln1270Arg
|
|
XM_017011104.1:c.3779A>G
|
XP_016866593.1:p.Gln1260Arg
|
|
XM_017011105.2:c.3749A>G
|
XP_016866594.1:p.Gln1250Arg
|
|
XM_017011106.2:c.3620A>G
|
XP_016866595.1:p.Gln1207Arg
|
|
XM_017011107.2:c.3599A>G
|
XP_016866596.1:p.Gln1200Arg
|
|
XR_002956289.1:n.3991A>G
|
|
|
NM_001363725.2:c.1448A>G
|
NP_001350654.1:p.Gln483Arg
|
|
NM_001371656.1:c.3827A>G
|
NP_001358585.1:p.Gln1276Arg
|
|
NM_001374820.1:c.3827A>G
|
NP_001361749.1:p.Gln1276Arg
|
|
NM_001374828.1:c.3947A>G
MANE Select
|
NP_001361757.1:p.Gln1316Arg
|
|
NM_017519.3:c.3788A>G
|
NP_059989.3:p.Gln1263Arg
|
|