ENST00000350026.11:c.4592A=
|
ENSP00000055163.8:p.Gln1531=
|
|
ENST00000414678.8:c.4661A=
|
ENSP00000412835.3:p.Gln1554=
|
|
ENST00000637015.2:c.4880A=
|
ENSP00000489729.2:p.Gln1627=
|
|
ENST00000346085.10:c.4631A=
|
ENSP00000344546.5:p.Gln1544=
|
|
ENST00000350026.10:c.4343A=
|
ENSP00000055163.7:p.Gln1448=
|
|
ENST00000414678.7:c.2909A=
|
ENSP00000412835.2:p.Gln970=
|
|
ENST00000635849.1:c.2072A=
|
ENSP00000490948.1:p.Gln691=
|
|
ENST00000635957.1:c.1703A=
|
ENSP00000490385.1:p.Gln568=
|
|
ENST00000636227.1:n.3214A=
|
|
|
ENST00000636254.1:n.671A=
|
|
|
ENST00000636930.2:c.4751A=
MANE Select
|
ENSP00000490491.2:p.Gln1584=
|
|
ENST00000636940.1:n.2748A=
|
|
|
ENST00000637015.1:c.2119A=
|
|
|
ENST00000637568.1:c.2033A=
|
|
|
ENST00000637741.1:n.1417A=
|
|
|
ENST00000637810.1:c.2093A=
|
ENSP00000489636.1:p.Gln698=
|
|
ENST00000637904.1:c.2252A=
|
ENSP00000490550.1:p.Gln751=
|
|
ENST00000647938.1:c.4382A=
|
ENSP00000498155.1:p.Gln1461=
|
|
ENST00000346085.9:c.4382A=
|
ENSP00000344546.4:p.Gln1461=
|
|
ENST00000350026.9:c.4343A=
|
ENSP00000055163.7:p.Gln1448=
|
|
ENST00000414678.6:c.2909A=
|
ENSP00000412835.2:p.Gln970=
|
|
NM_017519.2:c.4343A=
|
NP_059989.2:p.Gln1448=
|
|
NM_020732.3:c.4382A=
|
NP_065783.3:p.Gln1461=
|
|
XM_005267069.3:c.4502A=
|
XP_005267126.2:p.Gln1501=
|
|
XM_011535984.1:c.3581A=
|
XP_011534286.1:p.Gln1194=
|
|
XM_011535985.1:c.3401A=
|
XP_011534287.1:p.Gln1134=
|
|
XM_011535986.1:c.3161A=
|
XP_011534288.1:p.Gln1054=
|
|
XM_011535987.1:c.2780A=
|
XP_011534289.1:p.Gln927=
|
|
XM_011535988.1:c.1643A=
|
XP_011534290.1:p.Gln548=
|
|
NM_001346813.1:c.4502A=
|
NP_001333742.1:p.Gln1501=
|
|
NM_001363725.1:c.2252A=
|
NP_001350654.1:p.Gln751=
|
|
XM_011535984.2:c.4712A=
|
XP_011534286.2:p.Gln1571=
|
|
XM_011535988.3:c.1643A=
|
XP_011534290.1:p.Gln548=
|
|
XM_017011103.2:c.4613A=
|
XP_016866592.1:p.Gln1538=
|
|
XM_017011104.1:c.4583A=
|
XP_016866593.1:p.Gln1528=
|
|
XM_017011105.2:c.4553A=
|
XP_016866594.1:p.Gln1518=
|
|
XM_017011106.2:c.4424A=
|
XP_016866595.1:p.Gln1475=
|
|
XM_017011107.2:c.4403A=
|
XP_016866596.1:p.Gln1468=
|
|
XR_002956289.1:n.4698A=
|
|
|
NM_001363725.2:c.2252A=
|
NP_001350654.1:p.Gln751=
|
|
NM_001371656.1:c.4631A=
|
NP_001358585.1:p.Gln1544=
|
|
NM_001374820.1:c.4631A=
|
NP_001361749.1:p.Gln1544=
|
|
NM_001374828.1:c.4751A=
MANE Select
|
NP_001361757.1:p.Gln1584=
|
|
NM_017519.3:c.4592A=
|
NP_059989.3:p.Gln1531=
|
|