|
ENST00000348911.11:c.3890G>A
|
ENSP00000252027.8:p.Arg1297Gln
|
|
|
ENST00000470434.2:n.290G>A
|
|
|
|
ENST00000684986.1:c.3971G>A
|
ENSP00000509117.1:p.Arg1324Gln
|
|
|
ENST00000685180.1:n.2488+3924G>A
|
|
|
|
ENST00000685390.1:n.1936G>A
|
|
|
|
ENST00000685592.1:c.202G>A
|
|
|
|
ENST00000685809.1:c.3881G>A
|
ENSP00000508863.1:p.Arg1294Gln
|
|
|
ENST00000686029.1:c.64G>A
|
|
|
|
ENST00000686191.1:n.3168G>A
|
|
|
|
ENST00000686222.1:c.*3390G>A
|
ENSP00000508737.1:n.*3390G>A
|
|
|
ENST00000686321.1:c.64G>A
|
|
|
|
ENST00000686427.1:c.*903G>A
|
ENSP00000510379.1:n.*903G>A
|
|
|
ENST00000686758.1:n.1630G>A
|
|
|
|
ENST00000686801.1:c.3956G>A
|
ENSP00000509915.1:p.Arg1319Gln
|
|
|
ENST00000686826.1:n.285G>A
|
|
|
|
ENST00000687016.1:c.3869G>A
|
ENSP00000509074.1:p.Arg1290Gln
|
|
|
ENST00000687704.1:c.*1693G>A
|
ENSP00000510454.1:n.*1693G>A
|
|
|
ENST00000688066.1:c.3968G>A
|
ENSP00000510782.1:p.Arg1323Gln
|
|
|
ENST00000688124.1:c.*2884G>A
|
ENSP00000510645.1:n.*2884G>A
|
|
|
ENST00000688848.1:c.*3312G>A
|
ENSP00000509419.1:n.*3312G>A
|
|
|
ENST00000688985.1:c.969G>A
|
ENSP00000510477.1:p.Pro323=
|
|
|
ENST00000689129.1:c.3893G>A
|
ENSP00000510414.1:p.Arg1298Gln
|
|
|
ENST00000689177.1:n.4607G>A
|
|
|
|
ENST00000689849.1:c.64G>A
|
|
|
|
ENST00000689981.1:c.3968G>A
|
ENSP00000509035.1:p.Arg1323Gln
|
|
|
ENST00000690369.1:n.3986G>A
|
|
|
|
ENST00000690590.1:n.1015G>A
|
|
|
|
ENST00000690990.1:c.3962G>A
|
ENSP00000510461.1:p.Arg1321Gln
|
|
|
ENST00000691233.1:c.3887G>A
|
ENSP00000509215.1:p.Arg1296Gln
|
|
|
ENST00000691306.1:c.64G>A
|
|
|
|
ENST00000691345.1:n.2004G>A
|
|
|
|
ENST00000691792.1:c.3968G>A
|
ENSP00000509911.1:p.Arg1323Gln
|
|
|
ENST00000691959.1:n.4054G>A
|
|
|
|
ENST00000692844.1:n.1052G>A
|
|
|
|
ENST00000692946.1:c.64G>A
|
|
|
|
ENST00000693052.1:c.3986G>A
|
ENSP00000509558.1:p.Arg1329Gln
|
|
|
ENST00000693289.1:n.1127G>A
|
|
|
|
ENST00000693440.1:c.3965G>A
|
ENSP00000509462.1:p.Arg1322Gln
|
|
|
ENST00000693499.1:n.4893G>A
|
|
|
|
ENST00000693591.1:n.2072G>A
|
|
|
|
ENST00000380817.8:c.3968G>A
MANE Select
|
ENSP00000370196.2:p.Arg1323Gln
|
|
|
ENST00000348911.10:c.3893G>A
|
ENSP00000252027.7:p.Arg1298Gln
|
|
|
ENST00000380817.7:c.3968G>A
|
ENSP00000370196.2:p.Arg1323Gln
|
|
|
ENST00000476293.1:n.378G>A
|
|
|
|
NM_002972.3:c.3968G>A
|
NP_002963.2:p.Arg1323Gln
|
|
|
XM_005261931.1:c.3971G>A
|
XP_005261988.1:p.Arg1324Gln
|
|
|
XM_005261935.1:c.3890G>A
|
XP_005261992.1:p.Arg1297Gln
|
|
|
XM_011530707.1:c.4070G>A
|
XP_011529009.1:p.Arg1357Gln
|
|
|
XM_011530708.1:c.4022G>A
|
XP_011529010.1:p.Arg1341Gln
|
|
|
XM_011530709.1:c.3998G>A
|
XP_011529011.1:p.Arg1333Gln
|
|
|
XM_011530710.1:c.3995G>A
|
XP_011529012.1:p.Arg1332Gln
|
|
|
XM_011530711.1:c.3995G>A
|
XP_011529013.1:p.Arg1332Gln
|
|
|
XR_938344.1:n.4088G>A
|
|
|
|
NM_001365819.1:c.3893G>A
|
NP_001352748.1:p.Arg1298Gln
|
|
|
XM_005261935.2:c.3890G>A
|
XP_005261992.1:p.Arg1297Gln
|
|
|
XM_011530709.2:c.3998G>A
|
XP_011529011.1:p.Arg1333Gln
|
|
|
XM_011530710.2:c.3995G>A
|
XP_011529012.1:p.Arg1332Gln
|
|
|
XM_017028905.2:c.3920G>A
|
XP_016884394.1:p.Arg1307Gln
|
|
|
NM_002972.4:c.3968G>A
MANE Select
|
NP_002963.2:p.Arg1323Gln
|
|
