|
ENST00000348911.11:c.3827-442T>C
|
ENSP00000252027.8:n.3827-442T>C
|
|
|
ENST00000470434.2:n.227-442T>C
|
|
|
|
ENST00000684986.1:c.3830-4T>C
|
ENSP00000509117.1:n.3830-4T>C
|
|
|
ENST00000685180.1:n.2488+3419T>C
|
|
|
|
ENST00000685390.1:n.1873-442T>C
|
|
|
|
ENST00000685592.1:c.139-442T>C
|
|
|
|
ENST00000685809.1:c.3818-442T>C
|
ENSP00000508863.1:n.3818-442T>C
|
|
|
ENST00000686191.1:n.2663T>C
|
|
|
|
ENST00000686222.1:c.*3249-4T>C
|
ENSP00000508737.1:n.*3249-4T>C
|
|
|
ENST00000686427.1:c.*840-442T>C
|
ENSP00000510379.1:n.*840-442T>C
|
|
|
ENST00000686758.1:n.1125T>C
|
|
|
|
ENST00000686801.1:c.3815-4T>C
|
ENSP00000509915.1:n.3815-4T>C
|
|
|
ENST00000686826.1:n.144-4T>C
|
|
|
|
ENST00000687016.1:c.3806-442T>C
|
ENSP00000509074.1:n.3806-442T>C
|
|
|
ENST00000687704.1:c.*1630-442T>C
|
ENSP00000510454.1:n.*1630-442T>C
|
|
|
ENST00000687861.1:n.385-4T>C
|
|
|
|
ENST00000688066.1:c.3827-4T>C
|
ENSP00000510782.1:n.3827-4T>C
|
|
|
ENST00000688124.1:c.*2821-442T>C
|
ENSP00000510645.1:n.*2821-442T>C
|
|
|
ENST00000688848.1:c.*3249-442T>C
|
ENSP00000509419.1:n.*3249-442T>C
|
|
|
ENST00000688985.1:c.833-4T>C
|
ENSP00000510477.1:n.833-4T>C
|
|
|
ENST00000689129.1:c.3830-442T>C
|
ENSP00000510414.1:n.3830-442T>C
|
|
|
ENST00000689177.1:n.4102T>C
|
|
|
|
ENST00000689981.1:c.3827-4T>C
|
ENSP00000509035.1:n.3827-4T>C
|
|
|
ENST00000690369.1:n.3845-4T>C
|
|
|
|
ENST00000690590.1:n.874-4T>C
|
|
|
|
ENST00000690990.1:c.3821-4T>C
|
ENSP00000510461.1:n.3821-4T>C
|
|
|
ENST00000691233.1:c.3824-442T>C
|
ENSP00000509215.1:n.3824-442T>C
|
|
|
ENST00000691345.1:n.1941-442T>C
|
|
|
|
ENST00000691792.1:c.3827-4T>C
|
ENSP00000509911.1:n.3827-4T>C
|
|
|
ENST00000691959.1:n.3991-442T>C
|
|
|
|
ENST00000692844.1:n.989-442T>C
|
|
|
|
ENST00000693052.1:c.3845-4T>C
|
ENSP00000509558.1:n.3845-4T>C
|
|
|
ENST00000693289.1:n.626-4T>C
|
|
|
|
ENST00000693440.1:c.3824-4T>C
|
ENSP00000509462.1:n.3824-4T>C
|
|
|
ENST00000693499.1:n.4392-4T>C
|
|
|
|
ENST00000693591.1:n.1567T>C
|
|
|
|
ENST00000380817.8:c.3827-4T>C
MANE Select
|
ENSP00000370196.2:n.3827-4T>C
|
|
|
ENST00000348911.10:c.3830-442T>C
|
ENSP00000252027.7:n.3830-442T>C
|
|
|
ENST00000380817.7:c.3827-4T>C
|
ENSP00000370196.2:n.3827-4T>C
|
|
|
ENST00000476293.1:n.233T>C
|
|
|
|
NM_002972.3:c.3827-4T>C
|
NP_002963.2:n.3827-4T>C
|
|
|
XM_005261931.1:c.3830-4T>C
|
XP_005261988.1:n.3830-4T>C
|
|
|
XM_005261935.1:c.3827-442T>C
|
XP_005261992.1:n.3827-442T>C
|
|
|
XM_011530707.1:c.3929-4T>C
|
XP_011529009.1:n.3929-4T>C
|
|
|
XM_011530708.1:c.3881-4T>C
|
XP_011529010.1:n.3881-4T>C
|
|
|
XM_011530709.1:c.3857-4T>C
|
XP_011529011.1:n.3857-4T>C
|
|
|
XM_011530710.1:c.3854-4T>C
|
XP_011529012.1:n.3854-4T>C
|
|
|
XM_011530711.1:c.3932-442T>C
|
XP_011529013.1:n.3932-442T>C
|
|
|
XR_938344.1:n.3947-4T>C
|
|
|
|
NM_001365819.1:c.3830-442T>C
|
NP_001352748.1:n.3830-442T>C
|
|
|
XM_005261935.2:c.3827-442T>C
|
XP_005261992.1:n.3827-442T>C
|
|
|
XM_011530709.2:c.3857-4T>C
|
XP_011529011.1:n.3857-4T>C
|
|
|
XM_011530710.2:c.3854-4T>C
|
XP_011529012.1:n.3854-4T>C
|
|
|
XM_017028905.2:c.3857-442T>C
|
XP_016884394.1:n.3857-442T>C
|
|
|
NM_002972.4:c.3827-4T>C
MANE Select
|
NP_002963.2:n.3827-4T>C
|
|
