ENST00000350026.11:c.4591C>G
|
ENSP00000055163.8:p.Gln1531Glu
|
|
ENST00000414678.8:c.4660C>G
|
ENSP00000412835.3:p.Gln1554Glu
|
|
ENST00000637015.2:c.4879C>G
|
ENSP00000489729.2:p.Gln1627Glu
|
|
ENST00000346085.10:c.4630C>G
|
ENSP00000344546.5:p.Gln1544Glu
|
|
ENST00000350026.10:c.4342C>G
|
ENSP00000055163.7:p.Gln1448Glu
|
|
ENST00000414678.7:c.2908C>G
|
ENSP00000412835.2:p.Gln970Glu
|
|
ENST00000635849.1:c.2071C>G
|
ENSP00000490948.1:p.Gln691Glu
|
|
ENST00000635957.1:c.1702C>G
|
ENSP00000490385.1:p.Gln568Glu
|
|
ENST00000636227.1:n.3213C>G
|
|
|
ENST00000636254.1:n.670C>G
|
|
|
ENST00000636930.2:c.4750C>G
MANE Select
|
ENSP00000490491.2:p.Gln1584Glu
|
|
ENST00000636940.1:n.2747C>G
|
|
|
ENST00000637015.1:c.2118C>G
|
|
|
ENST00000637568.1:c.2032C>G
|
|
|
ENST00000637741.1:n.1416C>G
|
|
|
ENST00000637810.1:c.2092C>G
|
ENSP00000489636.1:p.Gln698Glu
|
|
ENST00000637904.1:c.2251C>G
|
ENSP00000490550.1:p.Gln751Glu
|
|
ENST00000647938.1:c.4381C>G
|
ENSP00000498155.1:p.Gln1461Glu
|
|
ENST00000346085.9:c.4381C>G
|
ENSP00000344546.4:p.Gln1461Glu
|
|
ENST00000350026.9:c.4342C>G
|
ENSP00000055163.7:p.Gln1448Glu
|
|
ENST00000414678.6:c.2908C>G
|
ENSP00000412835.2:p.Gln970Glu
|
|
NM_017519.2:c.4342C>G
|
NP_059989.2:p.Gln1448Glu
|
|
NM_020732.3:c.4381C>G
|
NP_065783.3:p.Gln1461Glu
|
|
XM_005267069.3:c.4501C>G
|
XP_005267126.2:p.Gln1501Glu
|
|
XM_011535984.1:c.3580C>G
|
XP_011534286.1:p.Gln1194Glu
|
|
XM_011535985.1:c.3400C>G
|
XP_011534287.1:p.Gln1134Glu
|
|
XM_011535986.1:c.3160C>G
|
XP_011534288.1:p.Gln1054Glu
|
|
XM_011535987.1:c.2779C>G
|
XP_011534289.1:p.Gln927Glu
|
|
XM_011535988.1:c.1642C>G
|
XP_011534290.1:p.Gln548Glu
|
|
NM_001346813.1:c.4501C>G
|
NP_001333742.1:p.Gln1501Glu
|
|
NM_001363725.1:c.2251C>G
|
NP_001350654.1:p.Gln751Glu
|
|
XM_011535984.2:c.4711C>G
|
XP_011534286.2:p.Gln1571Glu
|
|
XM_011535988.3:c.1642C>G
|
XP_011534290.1:p.Gln548Glu
|
|
XM_017011103.2:c.4612C>G
|
XP_016866592.1:p.Gln1538Glu
|
|
XM_017011104.1:c.4582C>G
|
XP_016866593.1:p.Gln1528Glu
|
|
XM_017011105.2:c.4552C>G
|
XP_016866594.1:p.Gln1518Glu
|
|
XM_017011106.2:c.4423C>G
|
XP_016866595.1:p.Gln1475Glu
|
|
XM_017011107.2:c.4402C>G
|
XP_016866596.1:p.Gln1468Glu
|
|
XR_002956289.1:n.4697C>G
|
|
|
NM_001363725.2:c.2251C>G
|
NP_001350654.1:p.Gln751Glu
|
|
NM_001371656.1:c.4630C>G
|
NP_001358585.1:p.Gln1544Glu
|
|
NM_001374820.1:c.4630C>G
|
NP_001361749.1:p.Gln1544Glu
|
|
NM_001374828.1:c.4750C>G
MANE Select
|
NP_001361757.1:p.Gln1584Glu
|
|
NM_017519.3:c.4591C>G
|
NP_059989.3:p.Gln1531Glu
|
|