ENST00000350026.11:c.4666C>G
|
ENSP00000055163.8:p.Gln1556Glu
|
|
ENST00000414678.8:c.4735C>G
|
ENSP00000412835.3:p.Gln1579Glu
|
|
ENST00000637015.2:c.4954C>G
|
ENSP00000489729.2:p.Gln1652Glu
|
|
ENST00000346085.10:c.4705C>G
|
ENSP00000344546.5:p.Gln1569Glu
|
|
ENST00000350026.10:c.4417C>G
|
ENSP00000055163.7:p.Gln1473Glu
|
|
ENST00000414678.7:c.2983C>G
|
ENSP00000412835.2:p.Gln995Glu
|
|
ENST00000635849.1:c.2146C>G
|
ENSP00000490948.1:p.Gln716Glu
|
|
ENST00000635957.1:c.1777C>G
|
ENSP00000490385.1:p.Gln593Glu
|
|
ENST00000636227.1:n.3288C>G
|
|
|
ENST00000636254.1:n.745C>G
|
|
|
ENST00000636930.2:c.4825C>G
MANE Select
|
ENSP00000490491.2:p.Gln1609Glu
|
|
ENST00000636940.1:n.2822C>G
|
|
|
ENST00000637015.1:c.2193C>G
|
|
|
ENST00000637568.1:c.2107C>G
|
|
|
ENST00000637741.1:n.1491C>G
|
|
|
ENST00000637810.1:c.2167C>G
|
ENSP00000489636.1:p.Gln723Glu
|
|
ENST00000637904.1:c.2326C>G
|
ENSP00000490550.1:p.Gln776Glu
|
|
ENST00000647938.1:c.4456C>G
|
ENSP00000498155.1:p.Gln1486Glu
|
|
ENST00000346085.9:c.4456C>G
|
ENSP00000344546.4:p.Gln1486Glu
|
|
ENST00000350026.9:c.4417C>G
|
ENSP00000055163.7:p.Gln1473Glu
|
|
ENST00000414678.6:c.2983C>G
|
ENSP00000412835.2:p.Gln995Glu
|
|
NM_017519.2:c.4417C>G
|
NP_059989.2:p.Gln1473Glu
|
|
NM_020732.3:c.4456C>G
|
NP_065783.3:p.Gln1486Glu
|
|
XM_005267069.3:c.4576C>G
|
XP_005267126.2:p.Gln1526Glu
|
|
XM_011535984.1:c.3655C>G
|
XP_011534286.1:p.Gln1219Glu
|
|
XM_011535985.1:c.3475C>G
|
XP_011534287.1:p.Gln1159Glu
|
|
XM_011535986.1:c.3235C>G
|
XP_011534288.1:p.Gln1079Glu
|
|
XM_011535987.1:c.2854C>G
|
XP_011534289.1:p.Gln952Glu
|
|
XM_011535988.1:c.1717C>G
|
XP_011534290.1:p.Gln573Glu
|
|
NM_001346813.1:c.4576C>G
|
NP_001333742.1:p.Gln1526Glu
|
|
NM_001363725.1:c.2326C>G
|
NP_001350654.1:p.Gln776Glu
|
|
XM_011535984.2:c.4786C>G
|
XP_011534286.2:p.Gln1596Glu
|
|
XM_011535988.3:c.1717C>G
|
XP_011534290.1:p.Gln573Glu
|
|
XM_017011103.2:c.4687C>G
|
XP_016866592.1:p.Gln1563Glu
|
|
XM_017011104.1:c.4657C>G
|
XP_016866593.1:p.Gln1553Glu
|
|
XM_017011105.2:c.4627C>G
|
XP_016866594.1:p.Gln1543Glu
|
|
XM_017011106.2:c.4498C>G
|
XP_016866595.1:p.Gln1500Glu
|
|
XM_017011107.2:c.4477C>G
|
XP_016866596.1:p.Gln1493Glu
|
|
XR_002956289.1:n.4772C>G
|
|
|
NM_001363725.2:c.2326C>G
|
NP_001350654.1:p.Gln776Glu
|
|
NM_001371656.1:c.4705C>G
|
NP_001358585.1:p.Gln1569Glu
|
|
NM_001374820.1:c.4705C>G
|
NP_001361749.1:p.Gln1569Glu
|
|
NM_001374828.1:c.4825C>G
MANE Select
|
NP_001361757.1:p.Gln1609Glu
|
|
NM_017519.3:c.4666C>G
|
NP_059989.3:p.Gln1556Glu
|
|