ENST00000350026.11:c.3779A>G
|
ENSP00000055163.8:p.Gln1260Arg
|
|
ENST00000414678.8:c.3848A>G
|
ENSP00000412835.3:p.Gln1283Arg
|
|
ENST00000637015.2:c.4067A>G
|
ENSP00000489729.2:p.Gln1356Arg
|
|
ENST00000346085.10:c.3818A>G
|
ENSP00000344546.5:p.Gln1273Arg
|
|
ENST00000350026.10:c.3530A>G
|
ENSP00000055163.7:p.Gln1177Arg
|
|
ENST00000414678.7:c.2096A>G
|
ENSP00000412835.2:p.Gln699Arg
|
|
ENST00000635849.1:c.1259A>G
|
ENSP00000490948.1:p.Gln420Arg
|
|
ENST00000635957.1:c.893A>G
|
ENSP00000490385.1:p.Gln298Arg
|
|
ENST00000636930.2:c.3938A>G
MANE Select
|
ENSP00000490491.2:p.Gln1313Arg
|
|
ENST00000636940.1:n.1935A>G
|
|
|
ENST00000637015.1:c.1306A>G
|
|
|
ENST00000637568.1:c.1220A>G
|
|
|
ENST00000637741.1:n.604A>G
|
|
|
ENST00000637810.1:c.1280A>G
|
ENSP00000489636.1:p.Gln427Arg
|
|
ENST00000637904.1:c.1439A>G
|
ENSP00000490550.1:p.Gln480Arg
|
|
ENST00000647938.1:c.3569A>G
|
ENSP00000498155.1:p.Gln1190Arg
|
|
ENST00000346085.9:c.3569A>G
|
ENSP00000344546.4:p.Gln1190Arg
|
|
ENST00000350026.9:c.3530A>G
|
ENSP00000055163.7:p.Gln1177Arg
|
|
ENST00000414678.6:c.2096A>G
|
ENSP00000412835.2:p.Gln699Arg
|
|
NM_017519.2:c.3530A>G
|
NP_059989.2:p.Gln1177Arg
|
|
NM_020732.3:c.3569A>G
|
NP_065783.3:p.Gln1190Arg
|
|
XM_005267069.3:c.3689A>G
|
XP_005267126.2:p.Gln1230Arg
|
|
XM_011535984.1:c.2768A>G
|
XP_011534286.1:p.Gln923Arg
|
|
XM_011535985.1:c.2588A>G
|
XP_011534287.1:p.Gln863Arg
|
|
XM_011535986.1:c.2348A>G
|
XP_011534288.1:p.Gln783Arg
|
|
XM_011535987.1:c.1967A>G
|
XP_011534289.1:p.Gln656Arg
|
|
XM_011535988.1:c.830A>G
|
XP_011534290.1:p.Gln277Arg
|
|
NM_001346813.1:c.3689A>G
|
NP_001333742.1:p.Gln1230Arg
|
|
NM_001363725.1:c.1439A>G
|
NP_001350654.1:p.Gln480Arg
|
|
XM_011535984.2:c.3899A>G
|
XP_011534286.2:p.Gln1300Arg
|
|
XM_011535988.3:c.830A>G
|
XP_011534290.1:p.Gln277Arg
|
|
XM_017011103.2:c.3800A>G
|
XP_016866592.1:p.Gln1267Arg
|
|
XM_017011104.1:c.3770A>G
|
XP_016866593.1:p.Gln1257Arg
|
|
XM_017011105.2:c.3740A>G
|
XP_016866594.1:p.Gln1247Arg
|
|
XM_017011106.2:c.3611A>G
|
XP_016866595.1:p.Gln1204Arg
|
|
XM_017011107.2:c.3590A>G
|
XP_016866596.1:p.Gln1197Arg
|
|
XR_002956289.1:n.3982A>G
|
|
|
NM_001363725.2:c.1439A>G
|
NP_001350654.1:p.Gln480Arg
|
|
NM_001371656.1:c.3818A>G
|
NP_001358585.1:p.Gln1273Arg
|
|
NM_001374820.1:c.3818A>G
|
NP_001361749.1:p.Gln1273Arg
|
|
NM_001374828.1:c.3938A>G
MANE Select
|
NP_001361757.1:p.Gln1313Arg
|
|
NM_017519.3:c.3779A>G
|
NP_059989.3:p.Gln1260Arg
|
|