ENST00000350026.11:c.4525C>G
|
ENSP00000055163.8:p.Gln1509Glu
|
|
ENST00000414678.8:c.4594C>G
|
ENSP00000412835.3:p.Gln1532Glu
|
|
ENST00000637015.2:c.4813C>G
|
ENSP00000489729.2:p.Gln1605Glu
|
|
ENST00000346085.10:c.4564C>G
|
ENSP00000344546.5:p.Gln1522Glu
|
|
ENST00000350026.10:c.4276C>G
|
ENSP00000055163.7:p.Gln1426Glu
|
|
ENST00000414678.7:c.2842C>G
|
ENSP00000412835.2:p.Gln948Glu
|
|
ENST00000635849.1:c.2005C>G
|
ENSP00000490948.1:p.Gln669Glu
|
|
ENST00000635957.1:c.1636C>G
|
ENSP00000490385.1:p.Gln546Glu
|
|
ENST00000636227.1:n.3147C>G
|
|
|
ENST00000636254.1:n.604C>G
|
|
|
ENST00000636930.2:c.4684C>G
MANE Select
|
ENSP00000490491.2:p.Gln1562Glu
|
|
ENST00000636940.1:n.2681C>G
|
|
|
ENST00000637015.1:c.2052C>G
|
|
|
ENST00000637568.1:c.1966C>G
|
|
|
ENST00000637741.1:n.1350C>G
|
|
|
ENST00000637810.1:c.2026C>G
|
ENSP00000489636.1:p.Gln676Glu
|
|
ENST00000637904.1:c.2185C>G
|
ENSP00000490550.1:p.Gln729Glu
|
|
ENST00000647938.1:c.4315C>G
|
ENSP00000498155.1:p.Gln1439Glu
|
|
ENST00000346085.9:c.4315C>G
|
ENSP00000344546.4:p.Gln1439Glu
|
|
ENST00000350026.9:c.4276C>G
|
ENSP00000055163.7:p.Gln1426Glu
|
|
ENST00000414678.6:c.2842C>G
|
ENSP00000412835.2:p.Gln948Glu
|
|
NM_017519.2:c.4276C>G
|
NP_059989.2:p.Gln1426Glu
|
|
NM_020732.3:c.4315C>G
|
NP_065783.3:p.Gln1439Glu
|
|
XM_005267069.3:c.4435C>G
|
XP_005267126.2:p.Gln1479Glu
|
|
XM_011535984.1:c.3514C>G
|
XP_011534286.1:p.Gln1172Glu
|
|
XM_011535985.1:c.3334C>G
|
XP_011534287.1:p.Gln1112Glu
|
|
XM_011535986.1:c.3094C>G
|
XP_011534288.1:p.Gln1032Glu
|
|
XM_011535987.1:c.2713C>G
|
XP_011534289.1:p.Gln905Glu
|
|
XM_011535988.1:c.1576C>G
|
XP_011534290.1:p.Gln526Glu
|
|
NM_001346813.1:c.4435C>G
|
NP_001333742.1:p.Gln1479Glu
|
|
NM_001363725.1:c.2185C>G
|
NP_001350654.1:p.Gln729Glu
|
|
XM_011535984.2:c.4645C>G
|
XP_011534286.2:p.Gln1549Glu
|
|
XM_011535988.3:c.1576C>G
|
XP_011534290.1:p.Gln526Glu
|
|
XM_017011103.2:c.4546C>G
|
XP_016866592.1:p.Gln1516Glu
|
|
XM_017011104.1:c.4516C>G
|
XP_016866593.1:p.Gln1506Glu
|
|
XM_017011105.2:c.4486C>G
|
XP_016866594.1:p.Gln1496Glu
|
|
XM_017011106.2:c.4357C>G
|
XP_016866595.1:p.Gln1453Glu
|
|
XM_017011107.2:c.4336C>G
|
XP_016866596.1:p.Gln1446Glu
|
|
XR_002956289.1:n.4631C>G
|
|
|
NM_001363725.2:c.2185C>G
|
NP_001350654.1:p.Gln729Glu
|
|
NM_001371656.1:c.4564C>G
|
NP_001358585.1:p.Gln1522Glu
|
|
NM_001374820.1:c.4564C>G
|
NP_001361749.1:p.Gln1522Glu
|
|
NM_001374828.1:c.4684C>G
MANE Select
|
NP_001361757.1:p.Gln1562Glu
|
|
NM_017519.3:c.4525C>G
|
NP_059989.3:p.Gln1509Glu
|
|