ENST00000505435.4:n.776G>T
|
|
|
ENST00000505787.8:n.2660G>T
|
|
|
ENST00000509358.7:c.820G>T
|
ENSP00000420994.3:p.Asp274Tyr
|
|
ENST00000509539.3:c.82G>T
|
ENSP00000425474.3:p.Asp28Tyr
|
|
ENST00000510895.7:n.943G>T
|
|
|
ENST00000629193.3:c.706G>T
|
ENSP00000486535.2:p.Asp236Tyr
|
|
ENST00000681968.1:c.313G>T
|
ENSP00000508143.1:p.Asp105Tyr
|
|
ENST00000682045.1:c.676G>T
|
ENSP00000507329.1:p.Asp226Tyr
|
|
ENST00000682214.1:c.427G>T
|
ENSP00000507336.1:p.Asp143Tyr
|
|
ENST00000682499.1:n.1641G>T
|
|
|
ENST00000682541.1:c.820G>T
|
ENSP00000507673.1:p.Asp274Tyr
|
|
ENST00000682687.1:c.820G>T
|
ENSP00000507945.1:p.Asp274Tyr
|
|
ENST00000682727.1:c.820G>T
|
ENSP00000507393.1:p.Asp274Tyr
|
|
ENST00000682876.1:c.949G>T
|
ENSP00000508389.1:p.Asp317Tyr
|
|
ENST00000683098.1:c.803+2774G>T
|
ENSP00000507670.1:n.803+2774G>T
|
|
ENST00000683258.1:c.*541G>T
|
ENSP00000507448.1:n.*541G>T
|
|
ENST00000683339.1:c.604G>T
|
ENSP00000507758.1:p.Asp202Tyr
|
|
ENST00000683403.1:c.813+7G>T
|
ENSP00000507896.1:n.813+7G>T
|
|
ENST00000683429.1:c.427G>T
|
ENSP00000507697.1:p.Asp143Tyr
|
|
ENST00000683665.1:c.820G>T
|
ENSP00000507068.1:p.Asp274Tyr
|
|
ENST00000683789.1:c.706G>T
|
ENSP00000507012.1:p.Asp236Tyr
|
|
ENST00000683847.1:n.664G>T
|
|
|
ENST00000683882.1:c.820G>T
|
ENSP00000506735.1:p.Asp274Tyr
|
|
ENST00000684024.1:c.*491G>T
|
ENSP00000507175.1:n.*491G>T
|
|
ENST00000684254.1:c.*546G>T
|
ENSP00000508001.1:n.*546G>T
|
|
ENST00000684310.1:c.82G>T
|
ENSP00000507550.1:p.Asp28Tyr
|
|
ENST00000684530.1:c.82G>T
|
ENSP00000507439.1:p.Asp28Tyr
|
|
ENST00000684652.1:n.1822G>T
|
|
|
ENST00000340941.11:c.820G>T
MANE Select
|
ENSP00000343657.6:p.Asp274Tyr
|
|
ENST00000340941.10:c.820G>T
|
ENSP00000343657.6:p.Asp274Tyr
|
|
ENST00000505435.3:n.171G>T
|
|
|
ENST00000505787.7:n.634G>T
|
|
|
ENST00000509358.6:c.820G>T
|
ENSP00000420994.2:p.Asp274Tyr
|
|
ENST00000509539.2:c.145G>T
|
ENSP00000425474.2:p.Asp49Tyr
|
|
ENST00000510895.6:n.434G>T
|
|
|
ENST00000512218.6:c.706G>T
|
ENSP00000423202.2:p.Asp236Tyr
|
|
ENST00000629193.2:c.706G>T
|
ENSP00000486535.1:p.Asp236Tyr
|
|
NM_022132.4:c.820G>T
|
NP_071415.1:p.Asp274Tyr
|
|
XM_005248567.1:c.706G>T
|
XP_005248624.1:p.Asp236Tyr
|
|
XM_011543528.1:c.820G>T
|
XP_011541830.1:p.Asp274Tyr
|
|
XM_011543529.1:c.820G>T
|
XP_011541831.1:p.Asp274Tyr
|
|
NM_001363147.1:c.706G>T
|
NP_001350076.1:p.Asp236Tyr
|
|
XM_011543529.2:c.820G>T
|
XP_011541831.1:p.Asp274Tyr
|
|
XM_017009688.1:c.820G>T
|
XP_016865177.1:p.Asp274Tyr
|
|
XR_001742172.1:n.860G>T
|
|
|
NM_022132.5:c.820G>T
MANE Select
|
NP_071415.1:p.Asp274Tyr
|
|