|
ENST00000505435.4:n.873_874delinsCT
|
|
|
|
ENST00000505787.8:n.2757_2758delinsCT
|
|
|
|
ENST00000509358.7:c.917_918delinsCT
|
ENSP00000420994.3:p.Pro306=
|
|
|
ENST00000509539.3:c.179_180delinsCT
|
ENSP00000425474.3:p.Pro60=
|
|
|
ENST00000510895.7:n.1040_1041delinsCT
|
|
|
|
ENST00000629193.3:c.803_804delinsCT
|
ENSP00000486535.2:p.Pro268=
|
|
|
ENST00000681968.1:c.410_411delinsCT
|
ENSP00000508143.1:p.Pro137=
|
|
|
ENST00000682045.1:c.773_774delinsCT
|
ENSP00000507329.1:p.Pro258=
|
|
|
ENST00000682214.1:c.524_525delinsCT
|
ENSP00000507336.1:p.Pro175=
|
|
|
ENST00000682499.1:n.1738_1739delinsCT
|
|
|
|
ENST00000682541.1:c.917_918delinsCT
|
ENSP00000507673.1:p.Pro306=
|
|
|
ENST00000682687.1:c.917_918delinsCT
|
ENSP00000507945.1:p.Pro306=
|
|
|
ENST00000682727.1:c.917_918delinsCT
|
ENSP00000507393.1:p.Pro306=
|
|
|
ENST00000682876.1:c.1046_1047delinsCT
|
ENSP00000508389.1:p.Pro349=
|
|
|
ENST00000683098.1:c.803+2979_803+2980delinsCT
|
ENSP00000507670.1:n.803+2979_803+2980delinsCT
|
|
|
ENST00000683258.1:c.*638_*639delinsCT
|
ENSP00000507448.1:n.*638_*639delinsCT
|
|
|
ENST00000683339.1:c.701_702delinsCT
|
ENSP00000507758.1:p.Pro234=
|
|
|
ENST00000683403.1:c.827_828delinsCT
|
ENSP00000507896.1:p.Pro276=
|
|
|
ENST00000683429.1:c.524_525delinsCT
|
ENSP00000507697.1:p.Pro175=
|
|
|
ENST00000683665.1:c.917_918delinsCT
|
ENSP00000507068.1:p.Pro306=
|
|
|
ENST00000683789.1:c.803_804delinsCT
|
ENSP00000507012.1:p.Pro268=
|
|
|
ENST00000683847.1:n.761_762delinsCT
|
|
|
|
ENST00000683882.1:c.917_918delinsCT
|
ENSP00000506735.1:p.Pro306=
|
|
|
ENST00000684024.1:c.*588_*589delinsCT
|
ENSP00000507175.1:n.*588_*589delinsCT
|
|
|
ENST00000684254.1:c.*643_*644delinsCT
|
ENSP00000508001.1:n.*643_*644delinsCT
|
|
|
ENST00000684310.1:c.165+122_165+123delinsCT
|
ENSP00000507550.1:n.165+122_165+123delinsCT
|
|
|
ENST00000684530.1:c.179_180delinsCT
|
ENSP00000507439.1:p.Pro60=
|
|
|
ENST00000684652.1:n.1919_1920delinsCT
|
|
|
|
ENST00000340941.11:c.917_918delinsCT
MANE Select
|
ENSP00000343657.6:p.Pro306=
|
|
|
ENST00000340941.10:c.917_918delinsCT
|
ENSP00000343657.6:p.Pro306=
|
|
|
ENST00000505435.3:n.268_269delinsCT
|
|
|
|
ENST00000509358.6:c.917_918delinsCT
|
ENSP00000420994.2:p.Pro306=
|
|
|
ENST00000509539.2:c.242_243delinsCT
|
ENSP00000425474.2:p.Pro81=
|
|
|
ENST00000510895.6:n.531_532delinsCT
|
|
|
|
ENST00000512218.6:c.803_804delinsCT
|
ENSP00000423202.2:p.Pro268=
|
|
|
ENST00000629193.2:c.803_804delinsCT
|
ENSP00000486535.1:p.Pro268=
|
|
|
NM_022132.4:c.917_918delinsCT
|
NP_071415.1:p.Pro306=
|
|
|
XM_005248567.1:c.803_804delinsCT
|
XP_005248624.1:p.Pro268=
|
|
|
XM_011543528.1:c.917_918delinsCT
|
XP_011541830.1:p.Pro306=
|
|
|
XM_011543529.1:c.917_918delinsCT
|
XP_011541831.1:p.Pro306=
|
|
|
NM_001363147.1:c.803_804delinsCT
|
NP_001350076.1:p.Pro268=
|
|
|
XM_011543529.2:c.917_918delinsCT
|
XP_011541831.1:p.Pro306=
|
|
|
XM_017009688.1:c.917_918delinsCT
|
XP_016865177.1:p.Pro306=
|
|
|
XR_001742172.1:n.957_958delinsCT
|
|
|
|
NM_022132.5:c.917_918delinsCT
MANE Select
|
NP_071415.1:p.Pro306=
|
|
