ENST00000350026.11:c.4667A>G
|
ENSP00000055163.8:p.Gln1556Arg
|
|
ENST00000414678.8:c.4736A>G
|
ENSP00000412835.3:p.Gln1579Arg
|
|
ENST00000637015.2:c.4955A>G
|
ENSP00000489729.2:p.Gln1652Arg
|
|
ENST00000346085.10:c.4706A>G
|
ENSP00000344546.5:p.Gln1569Arg
|
|
ENST00000350026.10:c.4418A>G
|
ENSP00000055163.7:p.Gln1473Arg
|
|
ENST00000414678.7:c.2984A>G
|
ENSP00000412835.2:p.Gln995Arg
|
|
ENST00000635849.1:c.2147A>G
|
ENSP00000490948.1:p.Gln716Arg
|
|
ENST00000635957.1:c.1778A>G
|
ENSP00000490385.1:p.Gln593Arg
|
|
ENST00000636227.1:n.3289A>G
|
|
|
ENST00000636254.1:n.746A>G
|
|
|
ENST00000636930.2:c.4826A>G
MANE Select
|
ENSP00000490491.2:p.Gln1609Arg
|
|
ENST00000636940.1:n.2823A>G
|
|
|
ENST00000637015.1:c.2194A>G
|
|
|
ENST00000637568.1:c.2108A>G
|
|
|
ENST00000637741.1:n.1492A>G
|
|
|
ENST00000637810.1:c.2168A>G
|
ENSP00000489636.1:p.Gln723Arg
|
|
ENST00000637904.1:c.2327A>G
|
ENSP00000490550.1:p.Gln776Arg
|
|
ENST00000647938.1:c.4457A>G
|
ENSP00000498155.1:p.Gln1486Arg
|
|
ENST00000346085.9:c.4457A>G
|
ENSP00000344546.4:p.Gln1486Arg
|
|
ENST00000350026.9:c.4418A>G
|
ENSP00000055163.7:p.Gln1473Arg
|
|
ENST00000414678.6:c.2984A>G
|
ENSP00000412835.2:p.Gln995Arg
|
|
NM_017519.2:c.4418A>G
|
NP_059989.2:p.Gln1473Arg
|
|
NM_020732.3:c.4457A>G
|
NP_065783.3:p.Gln1486Arg
|
|
XM_005267069.3:c.4577A>G
|
XP_005267126.2:p.Gln1526Arg
|
|
XM_011535984.1:c.3656A>G
|
XP_011534286.1:p.Gln1219Arg
|
|
XM_011535985.1:c.3476A>G
|
XP_011534287.1:p.Gln1159Arg
|
|
XM_011535986.1:c.3236A>G
|
XP_011534288.1:p.Gln1079Arg
|
|
XM_011535987.1:c.2855A>G
|
XP_011534289.1:p.Gln952Arg
|
|
XM_011535988.1:c.1718A>G
|
XP_011534290.1:p.Gln573Arg
|
|
NM_001346813.1:c.4577A>G
|
NP_001333742.1:p.Gln1526Arg
|
|
NM_001363725.1:c.2327A>G
|
NP_001350654.1:p.Gln776Arg
|
|
XM_011535984.2:c.4787A>G
|
XP_011534286.2:p.Gln1596Arg
|
|
XM_011535988.3:c.1718A>G
|
XP_011534290.1:p.Gln573Arg
|
|
XM_017011103.2:c.4688A>G
|
XP_016866592.1:p.Gln1563Arg
|
|
XM_017011104.1:c.4658A>G
|
XP_016866593.1:p.Gln1553Arg
|
|
XM_017011105.2:c.4628A>G
|
XP_016866594.1:p.Gln1543Arg
|
|
XM_017011106.2:c.4499A>G
|
XP_016866595.1:p.Gln1500Arg
|
|
XM_017011107.2:c.4478A>G
|
XP_016866596.1:p.Gln1493Arg
|
|
XR_002956289.1:n.4773A>G
|
|
|
NM_001363725.2:c.2327A>G
|
NP_001350654.1:p.Gln776Arg
|
|
NM_001371656.1:c.4706A>G
|
NP_001358585.1:p.Gln1569Arg
|
|
NM_001374820.1:c.4706A>G
|
NP_001361749.1:p.Gln1569Arg
|
|
NM_001374828.1:c.4826A>G
MANE Select
|
NP_001361757.1:p.Gln1609Arg
|
|
NM_017519.3:c.4667A>G
|
NP_059989.3:p.Gln1556Arg
|
|