|
ENST00000505435.4:n.904A=
|
|
|
|
ENST00000505787.8:n.2788A=
|
|
|
|
ENST00000509358.7:c.948A=
|
ENSP00000420994.3:p.Glu316=
|
|
|
ENST00000509539.3:c.210A=
|
ENSP00000425474.3:p.Glu70=
|
|
|
ENST00000510895.7:n.1071A=
|
|
|
|
ENST00000629193.3:c.834A=
|
ENSP00000486535.2:p.Glu278=
|
|
|
ENST00000681968.1:c.441A=
|
ENSP00000508143.1:p.Glu147=
|
|
|
ENST00000682045.1:c.804A=
|
ENSP00000507329.1:p.Glu268=
|
|
|
ENST00000682214.1:c.555A=
|
ENSP00000507336.1:p.Glu185=
|
|
|
ENST00000682499.1:n.1769A=
|
|
|
|
ENST00000682541.1:c.948A=
|
ENSP00000507673.1:p.Glu316=
|
|
|
ENST00000682687.1:c.948A=
|
ENSP00000507945.1:p.Glu316=
|
|
|
ENST00000682727.1:c.948A=
|
ENSP00000507393.1:p.Glu316=
|
|
|
ENST00000682876.1:c.1077A=
|
ENSP00000508389.1:p.Glu359=
|
|
|
ENST00000683098.1:c.803+3010A=
|
ENSP00000507670.1:n.803+3010A=
|
|
|
ENST00000683258.1:c.*669A=
|
ENSP00000507448.1:n.*669A=
|
|
|
ENST00000683339.1:c.732A=
|
ENSP00000507758.1:p.Glu244=
|
|
|
ENST00000683403.1:c.858A=
|
ENSP00000507896.1:p.Glu286=
|
|
|
ENST00000683429.1:c.555A=
|
ENSP00000507697.1:p.Glu185=
|
|
|
ENST00000683665.1:c.948A=
|
ENSP00000507068.1:p.Glu316=
|
|
|
ENST00000683789.1:c.834A=
|
ENSP00000507012.1:p.Glu278=
|
|
|
ENST00000683847.1:n.792A=
|
|
|
|
ENST00000683882.1:c.948A=
|
ENSP00000506735.1:p.Glu316=
|
|
|
ENST00000684024.1:c.*619A=
|
ENSP00000507175.1:n.*619A=
|
|
|
ENST00000684254.1:c.*674A=
|
ENSP00000508001.1:n.*674A=
|
|
|
ENST00000684310.1:c.165+153A=
|
ENSP00000507550.1:n.165+153A=
|
|
|
ENST00000684530.1:c.210A=
|
ENSP00000507439.1:p.Glu70=
|
|
|
ENST00000684652.1:n.1950A=
|
|
|
|
ENST00000340941.11:c.948A=
MANE Select
|
ENSP00000343657.6:p.Glu316=
|
|
|
ENST00000340941.10:c.948A=
|
ENSP00000343657.6:p.Glu316=
|
|
|
ENST00000505435.3:n.299A=
|
|
|
|
ENST00000509358.6:c.948A=
|
ENSP00000420994.2:p.Glu316=
|
|
|
ENST00000509539.2:c.273A=
|
ENSP00000425474.2:p.Glu91=
|
|
|
ENST00000510895.6:n.562A=
|
|
|
|
ENST00000512218.6:c.834A=
|
ENSP00000423202.2:p.Glu278=
|
|
|
ENST00000629193.2:c.834A=
|
ENSP00000486535.1:p.Glu278=
|
|
|
NM_022132.4:c.948A=
|
NP_071415.1:p.Glu316=
|
|
|
XM_005248567.1:c.834A=
|
XP_005248624.1:p.Glu278=
|
|
|
XM_011543528.1:c.948A=
|
XP_011541830.1:p.Glu316=
|
|
|
XM_011543529.1:c.948A=
|
XP_011541831.1:p.Glu316=
|
|
|
NM_001363147.1:c.834A=
|
NP_001350076.1:p.Glu278=
|
|
|
XM_011543529.2:c.948A=
|
XP_011541831.1:p.Glu316=
|
|
|
XM_017009688.1:c.948A=
|
XP_016865177.1:p.Glu316=
|
|
|
XR_001742172.1:n.988A=
|
|
|
|
NM_022132.5:c.948A=
MANE Select
|
NP_071415.1:p.Glu316=
|
|
