|
ENST00000348911.11:c.4897C>T
|
ENSP00000252027.8:p.Arg1633Cys
|
|
|
ENST00000418590.4:c.571C>T
|
ENSP00000401538.2:p.Arg191Cys
|
|
|
ENST00000470434.2:n.1378C>T
|
|
|
|
ENST00000684986.1:c.4978C>T
|
ENSP00000509117.1:p.Arg1660Cys
|
|
|
ENST00000685180.1:n.2489-5930C>T
|
|
|
|
ENST00000685390.1:n.2926C>T
|
|
|
|
ENST00000685411.1:n.725C>T
|
|
|
|
ENST00000685459.1:c.127C>T
|
ENSP00000509511.1:p.Arg43Cys
|
|
|
ENST00000685592.1:c.1209C>T
|
|
|
|
ENST00000685809.1:c.4888C>T
|
ENSP00000508863.1:p.Arg1630Cys
|
|
|
ENST00000686191.1:n.4175C>T
|
|
|
|
ENST00000686222.1:c.*4397C>T
|
ENSP00000508737.1:n.*4397C>T
|
|
|
ENST00000686321.1:c.1071C>T
|
|
|
|
ENST00000686427.1:c.*1910C>T
|
ENSP00000510379.1:n.*1910C>T
|
|
|
ENST00000686758.1:n.2789C>T
|
|
|
|
ENST00000686801.1:c.4963C>T
|
ENSP00000509915.1:p.Arg1655Cys
|
|
|
ENST00000686826.1:n.1294C>T
|
|
|
|
ENST00000687016.1:c.4876C>T
|
ENSP00000509074.1:p.Arg1626Cys
|
|
|
ENST00000687704.1:c.*2771C>T
|
ENSP00000510454.1:n.*2771C>T
|
|
|
ENST00000688066.1:c.4975C>T
|
ENSP00000510782.1:p.Arg1659Cys
|
|
|
ENST00000688124.1:c.*3876C>T
|
ENSP00000510645.1:n.*3876C>T
|
|
|
ENST00000688381.1:c.127C>T
|
ENSP00000508847.1:p.Arg43Cys
|
|
|
ENST00000688848.1:c.*4319C>T
|
ENSP00000509419.1:n.*4319C>T
|
|
|
ENST00000688985.1:c.1976C>T
|
ENSP00000510477.1:n.1976C>T
|
|
|
ENST00000689129.1:c.4900C>T
|
ENSP00000510414.1:p.Arg1634Cys
|
|
|
ENST00000689177.1:n.6247C>T
|
|
|
|
ENST00000689849.1:c.1071C>T
|
|
|
|
ENST00000689981.1:c.4975C>T
|
ENSP00000509035.1:p.Arg1659Cys
|
|
|
ENST00000690369.1:n.4993C>T
|
|
|
|
ENST00000690590.1:n.2022C>T
|
|
|
|
ENST00000690990.1:c.4969C>T
|
ENSP00000510461.1:p.Arg1657Cys
|
|
|
ENST00000691233.1:c.4894C>T
|
ENSP00000509215.1:p.Arg1632Cys
|
|
|
ENST00000691306.1:c.1056C>T
|
|
|
|
ENST00000691345.1:n.2302+1636C>T
|
|
|
|
ENST00000691792.1:c.4963C>T
|
ENSP00000509911.1:p.Arg1655Cys
|
|
|
ENST00000691959.1:n.5694C>T
|
|
|
|
ENST00000692844.1:n.2059C>T
|
|
|
|
ENST00000692946.1:c.1071C>T
|
|
|
|
ENST00000693052.1:c.4993C>T
|
ENSP00000509558.1:p.Arg1665Cys
|
|
|
ENST00000693068.1:c.127C>T
|
ENSP00000509997.1:p.Arg43Cys
|
|
|
ENST00000693289.1:n.2134C>T
|
|
|
|
ENST00000693440.1:c.4972C>T
|
ENSP00000509462.1:p.Arg1658Cys
|
|
|
ENST00000693499.1:n.5971C>T
|
|
|
|
ENST00000693591.1:n.3783C>T
|
|
|
|
ENST00000380817.8:c.4975C>T
MANE Select
|
ENSP00000370196.2:p.Arg1659Cys
|
|
|
ENST00000348911.10:c.4900C>T
|
ENSP00000252027.7:p.Arg1634Cys
|
|
|
ENST00000380817.7:c.4975C>T
|
ENSP00000370196.2:p.Arg1659Cys
|
|
|
ENST00000418590.3:c.539C>T
|
|
|
|
ENST00000470434.1:n.1116C>T
|
|
|
|
NM_002972.3:c.4975C>T
|
NP_002963.2:p.Arg1659Cys
|
|
|
XM_005261931.1:c.4978C>T
|
XP_005261988.1:p.Arg1660Cys
|
|
|
XM_005261935.1:c.4897C>T
|
XP_005261992.1:p.Arg1633Cys
|
|
|
XM_011530707.1:c.5077C>T
|
XP_011529009.1:p.Arg1693Cys
|
|
|
XM_011530708.1:c.5029C>T
|
XP_011529010.1:p.Arg1677Cys
|
|
|
XM_011530709.1:c.5005C>T
|
XP_011529011.1:p.Arg1669Cys
|
|
|
XM_011530710.1:c.5002C>T
|
XP_011529012.1:p.Arg1668Cys
|
|
|
XM_011530711.1:c.5002C>T
|
XP_011529013.1:p.Arg1668Cys
|
|
|
XR_938344.1:n.5095C>T
|
|
|
|
NM_001365819.1:c.4900C>T
|
NP_001352748.1:p.Arg1634Cys
|
|
|
XM_005261935.2:c.4897C>T
|
XP_005261992.1:p.Arg1633Cys
|
|
|
XM_011530709.2:c.5005C>T
|
XP_011529011.1:p.Arg1669Cys
|
|
|
XM_011530710.2:c.5002C>T
|
XP_011529012.1:p.Arg1668Cys
|
|
|
XM_017028905.2:c.4927C>T
|
XP_016884394.1:p.Arg1643Cys
|
|
|
NM_002972.4:c.4975C>T
MANE Select
|
NP_002963.2:p.Arg1659Cys
|
|
