ENST00000350026.11:c.4242G>A
|
ENSP00000055163.8:p.Gln1414=
|
|
ENST00000414678.8:c.4311G>A
|
ENSP00000412835.3:p.Gln1437=
|
|
ENST00000637015.2:c.4530G>A
|
ENSP00000489729.2:p.Gln1510=
|
|
ENST00000346085.10:c.4281G>A
|
ENSP00000344546.5:p.Gln1427=
|
|
ENST00000350026.10:c.3993G>A
|
ENSP00000055163.7:p.Gln1331=
|
|
ENST00000414678.7:c.2559G>A
|
ENSP00000412835.2:p.Gln853=
|
|
ENST00000635849.1:c.1722G>A
|
ENSP00000490948.1:p.Gln574=
|
|
ENST00000635957.1:c.1353G>A
|
ENSP00000490385.1:p.Gln451=
|
|
ENST00000636227.1:n.2864G>A
|
|
|
ENST00000636254.1:n.321G>A
|
|
|
ENST00000636930.2:c.4401G>A
MANE Select
|
ENSP00000490491.2:p.Gln1467=
|
|
ENST00000636940.1:n.2398G>A
|
|
|
ENST00000637015.1:c.1769G>A
|
|
|
ENST00000637568.1:c.1683G>A
|
|
|
ENST00000637741.1:n.1067G>A
|
|
|
ENST00000637810.1:c.1743G>A
|
ENSP00000489636.1:p.Gln581=
|
|
ENST00000637904.1:c.1902G>A
|
ENSP00000490550.1:p.Gln634=
|
|
ENST00000647938.1:c.4032G>A
|
ENSP00000498155.1:p.Gln1344=
|
|
ENST00000346085.9:c.4032G>A
|
ENSP00000344546.4:p.Gln1344=
|
|
ENST00000350026.9:c.3993G>A
|
ENSP00000055163.7:p.Gln1331=
|
|
ENST00000414678.6:c.2559G>A
|
ENSP00000412835.2:p.Gln853=
|
|
NM_017519.2:c.3993G>A
|
NP_059989.2:p.Gln1331=
|
|
NM_020732.3:c.4032G>A
|
NP_065783.3:p.Gln1344=
|
|
XM_005267069.3:c.4152G>A
|
XP_005267126.2:p.Gln1384=
|
|
XM_011535984.1:c.3231G>A
|
XP_011534286.1:p.Gln1077=
|
|
XM_011535985.1:c.3051G>A
|
XP_011534287.1:p.Gln1017=
|
|
XM_011535986.1:c.2811G>A
|
XP_011534288.1:p.Gln937=
|
|
XM_011535987.1:c.2430G>A
|
XP_011534289.1:p.Gln810=
|
|
XM_011535988.1:c.1293G>A
|
XP_011534290.1:p.Gln431=
|
|
NM_001346813.1:c.4152G>A
|
NP_001333742.1:p.Gln1384=
|
|
NM_001363725.1:c.1902G>A
|
NP_001350654.1:p.Gln634=
|
|
XM_011535984.2:c.4362G>A
|
XP_011534286.2:p.Gln1454=
|
|
XM_011535988.3:c.1293G>A
|
XP_011534290.1:p.Gln431=
|
|
XM_017011103.2:c.4263G>A
|
XP_016866592.1:p.Gln1421=
|
|
XM_017011104.1:c.4233G>A
|
XP_016866593.1:p.Gln1411=
|
|
XM_017011105.2:c.4203G>A
|
XP_016866594.1:p.Gln1401=
|
|
XM_017011106.2:c.4074G>A
|
XP_016866595.1:p.Gln1358=
|
|
XM_017011107.2:c.4053G>A
|
XP_016866596.1:p.Gln1351=
|
|
XR_002956289.1:n.4427-1876G>A
|
|
|
NM_001363725.2:c.1902G>A
|
NP_001350654.1:p.Gln634=
|
|
NM_001371656.1:c.4281G>A
|
NP_001358585.1:p.Gln1427=
|
|
NM_001374820.1:c.4281G>A
|
NP_001361749.1:p.Gln1427=
|
|
NM_001374828.1:c.4401G>A
MANE Select
|
NP_001361757.1:p.Gln1467=
|
|
NM_017519.3:c.4242G>A
|
NP_059989.3:p.Gln1414=
|
|