ENST00000350026.11:c.3962G>A
|
ENSP00000055163.8:p.Arg1321Gln
|
|
ENST00000414678.8:c.4031G>A
|
ENSP00000412835.3:p.Arg1344Gln
|
|
ENST00000637015.2:c.4250G>A
|
ENSP00000489729.2:p.Arg1417Gln
|
|
ENST00000346085.10:c.4001G>A
|
ENSP00000344546.5:p.Arg1334Gln
|
|
ENST00000350026.10:c.3713G>A
|
ENSP00000055163.7:p.Arg1238Gln
|
|
ENST00000414678.7:c.2279G>A
|
ENSP00000412835.2:p.Arg760Gln
|
|
ENST00000635849.1:c.1442G>A
|
ENSP00000490948.1:p.Arg481Gln
|
|
ENST00000635957.1:c.1073G>A
|
ENSP00000490385.1:p.Arg358Gln
|
|
ENST00000636930.2:c.4121G>A
MANE Select
|
ENSP00000490491.2:p.Arg1374Gln
|
|
ENST00000636940.1:n.2118G>A
|
|
|
ENST00000637015.1:c.1489G>A
|
|
|
ENST00000637568.1:c.1403G>A
|
|
|
ENST00000637741.1:n.787G>A
|
|
|
ENST00000637810.1:c.1463G>A
|
ENSP00000489636.1:p.Arg488Gln
|
|
ENST00000637904.1:c.1622G>A
|
ENSP00000490550.1:p.Arg541Gln
|
|
ENST00000647938.1:c.3752G>A
|
ENSP00000498155.1:p.Arg1251Gln
|
|
ENST00000346085.9:c.3752G>A
|
ENSP00000344546.4:p.Arg1251Gln
|
|
ENST00000350026.9:c.3713G>A
|
ENSP00000055163.7:p.Arg1238Gln
|
|
ENST00000414678.6:c.2279G>A
|
ENSP00000412835.2:p.Arg760Gln
|
|
NM_017519.2:c.3713G>A
|
NP_059989.2:p.Arg1238Gln
|
|
NM_020732.3:c.3752G>A
|
NP_065783.3:p.Arg1251Gln
|
|
XM_005267069.3:c.3872G>A
|
XP_005267126.2:p.Arg1291Gln
|
|
XM_011535984.1:c.2951G>A
|
XP_011534286.1:p.Arg984Gln
|
|
XM_011535985.1:c.2771G>A
|
XP_011534287.1:p.Arg924Gln
|
|
XM_011535986.1:c.2531G>A
|
XP_011534288.1:p.Arg844Gln
|
|
XM_011535987.1:c.2150G>A
|
XP_011534289.1:p.Arg717Gln
|
|
XM_011535988.1:c.1013G>A
|
XP_011534290.1:p.Arg338Gln
|
|
NM_001346813.1:c.3872G>A
|
NP_001333742.1:p.Arg1291Gln
|
|
NM_001363725.1:c.1622G>A
|
NP_001350654.1:p.Arg541Gln
|
|
XM_011535984.2:c.4082G>A
|
XP_011534286.2:p.Arg1361Gln
|
|
XM_011535988.3:c.1013G>A
|
XP_011534290.1:p.Arg338Gln
|
|
XM_017011103.2:c.3983G>A
|
XP_016866592.1:p.Arg1328Gln
|
|
XM_017011104.1:c.3953G>A
|
XP_016866593.1:p.Arg1318Gln
|
|
XM_017011105.2:c.3923G>A
|
XP_016866594.1:p.Arg1308Gln
|
|
XM_017011106.2:c.3794G>A
|
XP_016866595.1:p.Arg1265Gln
|
|
XM_017011107.2:c.3773G>A
|
XP_016866596.1:p.Arg1258Gln
|
|
XR_002956289.1:n.4165G>A
|
|
|
NM_001363725.2:c.1622G>A
|
NP_001350654.1:p.Arg541Gln
|
|
NM_001371656.1:c.4001G>A
|
NP_001358585.1:p.Arg1334Gln
|
|
NM_001374820.1:c.4001G>A
|
NP_001361749.1:p.Arg1334Gln
|
|
NM_001374828.1:c.4121G>A
MANE Select
|
NP_001361757.1:p.Arg1374Gln
|
|
NM_017519.3:c.3962G>A
|
NP_059989.3:p.Arg1321Gln
|
|