|
ENST00000505435.4:n.770G=
|
|
|
|
ENST00000505787.8:n.2654G=
|
|
|
|
ENST00000509358.7:c.814G=
|
ENSP00000420994.3:p.Val272=
|
|
|
ENST00000509539.3:c.76G=
|
ENSP00000425474.3:p.Val26=
|
|
|
ENST00000510895.7:n.937G=
|
|
|
|
ENST00000629193.3:c.700G=
|
ENSP00000486535.2:p.Val234=
|
|
|
ENST00000681968.1:c.307G=
|
ENSP00000508143.1:p.Val103=
|
|
|
ENST00000682045.1:c.670G=
|
ENSP00000507329.1:p.Val224=
|
|
|
ENST00000682214.1:c.421G=
|
ENSP00000507336.1:p.Val141=
|
|
|
ENST00000682499.1:n.1635G=
|
|
|
|
ENST00000682541.1:c.814G=
|
ENSP00000507673.1:p.Val272=
|
|
|
ENST00000682687.1:c.814G=
|
ENSP00000507945.1:p.Val272=
|
|
|
ENST00000682727.1:c.814G=
|
ENSP00000507393.1:p.Val272=
|
|
|
ENST00000682876.1:c.943G=
|
ENSP00000508389.1:p.Val315=
|
|
|
ENST00000683098.1:c.803+2768G=
|
ENSP00000507670.1:n.803+2768G=
|
|
|
ENST00000683258.1:c.*535G=
|
ENSP00000507448.1:n.*535G=
|
|
|
ENST00000683339.1:c.598G=
|
ENSP00000507758.1:p.Val200=
|
|
|
ENST00000683403.1:c.813+1G=
|
ENSP00000507896.1:n.813+1G=
|
|
|
ENST00000683429.1:c.421G=
|
ENSP00000507697.1:p.Val141=
|
|
|
ENST00000683665.1:c.814G=
|
ENSP00000507068.1:p.Val272=
|
|
|
ENST00000683789.1:c.700G=
|
ENSP00000507012.1:p.Val234=
|
|
|
ENST00000683847.1:n.658G=
|
|
|
|
ENST00000683882.1:c.814G=
|
ENSP00000506735.1:p.Val272=
|
|
|
ENST00000684024.1:c.*485G=
|
ENSP00000507175.1:n.*485G=
|
|
|
ENST00000684254.1:c.*540G=
|
ENSP00000508001.1:n.*540G=
|
|
|
ENST00000684310.1:c.76G=
|
ENSP00000507550.1:p.Val26=
|
|
|
ENST00000684530.1:c.76G=
|
ENSP00000507439.1:p.Val26=
|
|
|
ENST00000684652.1:n.1816G=
|
|
|
|
ENST00000340941.11:c.814G=
MANE Select
|
ENSP00000343657.6:p.Val272=
|
|
|
ENST00000340941.10:c.814G=
|
ENSP00000343657.6:p.Val272=
|
|
|
ENST00000505435.3:n.165G=
|
|
|
|
ENST00000505787.7:n.628G=
|
|
|
|
ENST00000509358.6:c.814G=
|
ENSP00000420994.2:p.Val272=
|
|
|
ENST00000509539.2:c.139G=
|
ENSP00000425474.2:p.Val47=
|
|
|
ENST00000510895.6:n.428G=
|
|
|
|
ENST00000512218.6:c.700G=
|
ENSP00000423202.2:p.Val234=
|
|
|
ENST00000629193.2:c.700G=
|
ENSP00000486535.1:p.Val234=
|
|
|
NM_022132.4:c.814G=
|
NP_071415.1:p.Val272=
|
|
|
XM_005248567.1:c.700G=
|
XP_005248624.1:p.Val234=
|
|
|
XM_011543528.1:c.814G=
|
XP_011541830.1:p.Val272=
|
|
|
XM_011543529.1:c.814G=
|
XP_011541831.1:p.Val272=
|
|
|
NM_001363147.1:c.700G=
|
NP_001350076.1:p.Val234=
|
|
|
XM_011543529.2:c.814G=
|
XP_011541831.1:p.Val272=
|
|
|
XM_017009688.1:c.814G=
|
XP_016865177.1:p.Val272=
|
|
|
XR_001742172.1:n.854G=
|
|
|
|
NM_022132.5:c.814G=
MANE Select
|
NP_071415.1:p.Val272=
|
|
