|
ENST00000348911.11:c.4734+21G>T
|
ENSP00000252027.8:n.4734+21G>T
|
|
|
ENST00000418590.4:c.444+21G>T
|
ENSP00000401538.2:n.444+21G>T
|
|
|
ENST00000470434.2:n.1215+21G>T
|
|
|
|
ENST00000684986.1:c.4815+21G>T
|
ENSP00000509117.1:n.4815+21G>T
|
|
|
ENST00000685180.1:n.2488+5741G>T
|
|
|
|
ENST00000685390.1:n.2780+21G>T
|
|
|
|
ENST00000685411.1:n.562+21G>T
|
|
|
|
ENST00000685592.1:c.1046+21G>T
|
|
|
|
ENST00000685809.1:c.4725+21G>T
|
ENSP00000508863.1:n.4725+21G>T
|
|
|
ENST00000686191.1:n.4012+21G>T
|
|
|
|
ENST00000686222.1:c.*4234+21G>T
|
ENSP00000508737.1:n.*4234+21G>T
|
|
|
ENST00000686321.1:c.908+21G>T
|
|
|
|
ENST00000686427.1:c.*1747+21G>T
|
ENSP00000510379.1:n.*1747+21G>T
|
|
|
ENST00000686758.1:n.2626+21G>T
|
|
|
|
ENST00000686801.1:c.4800+21G>T
|
ENSP00000509915.1:n.4800+21G>T
|
|
|
ENST00000686826.1:n.1131+21G>T
|
|
|
|
ENST00000687016.1:c.4713+21G>T
|
ENSP00000509074.1:n.4713+21G>T
|
|
|
ENST00000687704.1:c.*2558G>T
|
ENSP00000510454.1:n.*2558G>T
|
|
|
ENST00000688066.1:c.4812+21G>T
|
ENSP00000510782.1:n.4812+21G>T
|
|
|
ENST00000688124.1:c.*3730+21G>T
|
ENSP00000510645.1:n.*3730+21G>T
|
|
|
ENST00000688848.1:c.*4156+21G>T
|
ENSP00000509419.1:n.*4156+21G>T
|
|
|
ENST00000688985.1:c.1813+21G>T
|
ENSP00000510477.1:n.1813+21G>T
|
|
|
ENST00000689129.1:c.4737+21G>T
|
ENSP00000510414.1:n.4737+21G>T
|
|
|
ENST00000689177.1:n.6084+21G>T
|
|
|
|
ENST00000689849.1:c.908+21G>T
|
|
|
|
ENST00000689981.1:c.4812+21G>T
|
ENSP00000509035.1:n.4812+21G>T
|
|
|
ENST00000690369.1:n.4830+21G>T
|
|
|
|
ENST00000690590.1:n.1859+21G>T
|
|
|
|
ENST00000690990.1:c.4806+21G>T
|
ENSP00000510461.1:n.4806+21G>T
|
|
|
ENST00000691233.1:c.4731+21G>T
|
ENSP00000509215.1:n.4731+21G>T
|
|
|
ENST00000691306.1:c.893+21G>T
|
|
|
|
ENST00000691345.1:n.2302+1423G>T
|
|
|
|
ENST00000691792.1:c.4800+21G>T
|
ENSP00000509911.1:n.4800+21G>T
|
|
|
ENST00000691959.1:n.5531+21G>T
|
|
|
|
ENST00000692844.1:n.1896+21G>T
|
|
|
|
ENST00000692946.1:c.908+21G>T
|
|
|
|
ENST00000693052.1:c.4830+21G>T
|
ENSP00000509558.1:n.4830+21G>T
|
|
|
ENST00000693289.1:n.1971+21G>T
|
|
|
|
ENST00000693440.1:c.4809+21G>T
|
ENSP00000509462.1:n.4809+21G>T
|
|
|
ENST00000693499.1:n.5808+21G>T
|
|
|
|
ENST00000693591.1:n.3620+21G>T
|
|
|
|
ENST00000380817.8:c.4812+21G>T
MANE Select
|
ENSP00000370196.2:n.4812+21G>T
|
|
|
ENST00000348911.10:c.4737+21G>T
|
ENSP00000252027.7:n.4737+21G>T
|
|
|
ENST00000380817.7:c.4812+21G>T
|
ENSP00000370196.2:n.4812+21G>T
|
|
|
ENST00000418590.3:c.412+21G>T
|
|
|
|
ENST00000470434.1:n.953+21G>T
|
|
|
|
NM_002972.3:c.4812+21G>T
|
NP_002963.2:n.4812+21G>T
|
|
|
XM_005261931.1:c.4815+21G>T
|
XP_005261988.1:n.4815+21G>T
|
|
|
XM_005261935.1:c.4734+21G>T
|
XP_005261992.1:n.4734+21G>T
|
|
|
XM_011530707.1:c.4914+21G>T
|
XP_011529009.1:n.4914+21G>T
|
|
|
XM_011530708.1:c.4866+21G>T
|
XP_011529010.1:n.4866+21G>T
|
|
|
XM_011530709.1:c.4842+21G>T
|
XP_011529011.1:n.4842+21G>T
|
|
|
XM_011530710.1:c.4839+21G>T
|
XP_011529012.1:n.4839+21G>T
|
|
|
XM_011530711.1:c.4839+21G>T
|
XP_011529013.1:n.4839+21G>T
|
|
|
XR_938344.1:n.4932+21G>T
|
|
|
|
NM_001365819.1:c.4737+21G>T
|
NP_001352748.1:n.4737+21G>T
|
|
|
XM_005261935.2:c.4734+21G>T
|
XP_005261992.1:n.4734+21G>T
|
|
|
XM_011530709.2:c.4842+21G>T
|
XP_011529011.1:n.4842+21G>T
|
|
|
XM_011530710.2:c.4839+21G>T
|
XP_011529012.1:n.4839+21G>T
|
|
|
XM_017028905.2:c.4764+21G>T
|
XP_016884394.1:n.4764+21G>T
|
|
|
NM_002972.4:c.4812+21G>T
MANE Select
|
NP_002963.2:n.4812+21G>T
|
|
