ENST00000505435.4:n.826T>C
|
|
|
ENST00000505787.8:n.2710T>C
|
|
|
ENST00000509358.7:c.870T>C
|
ENSP00000420994.3:p.Val290=
|
|
ENST00000509539.3:c.132T>C
|
ENSP00000425474.3:p.Val44=
|
|
ENST00000510895.7:n.993T>C
|
|
|
ENST00000629193.3:c.756T>C
|
ENSP00000486535.2:p.Val252=
|
|
ENST00000681968.1:c.363T>C
|
ENSP00000508143.1:p.Val121=
|
|
ENST00000682045.1:c.726T>C
|
ENSP00000507329.1:p.Val242=
|
|
ENST00000682214.1:c.477T>C
|
ENSP00000507336.1:p.Val159=
|
|
ENST00000682499.1:n.1691T>C
|
|
|
ENST00000682541.1:c.870T>C
|
ENSP00000507673.1:p.Val290=
|
|
ENST00000682687.1:c.870T>C
|
ENSP00000507945.1:p.Val290=
|
|
ENST00000682727.1:c.870T>C
|
ENSP00000507393.1:p.Val290=
|
|
ENST00000682876.1:c.999T>C
|
ENSP00000508389.1:p.Val333=
|
|
ENST00000683098.1:c.803+2824T>C
|
ENSP00000507670.1:n.803+2824T>C
|
|
ENST00000683258.1:c.*591T>C
|
ENSP00000507448.1:n.*591T>C
|
|
ENST00000683339.1:c.654T>C
|
ENSP00000507758.1:p.Val218=
|
|
ENST00000683403.1:c.813+57T>C
|
ENSP00000507896.1:n.813+57T>C
|
|
ENST00000683429.1:c.477T>C
|
ENSP00000507697.1:p.Val159=
|
|
ENST00000683665.1:c.870T>C
|
ENSP00000507068.1:p.Val290=
|
|
ENST00000683789.1:c.756T>C
|
ENSP00000507012.1:p.Val252=
|
|
ENST00000683847.1:n.714T>C
|
|
|
ENST00000683882.1:c.870T>C
|
ENSP00000506735.1:p.Val290=
|
|
ENST00000684024.1:c.*541T>C
|
ENSP00000507175.1:n.*541T>C
|
|
ENST00000684254.1:c.*596T>C
|
ENSP00000508001.1:n.*596T>C
|
|
ENST00000684310.1:c.132T>C
|
ENSP00000507550.1:p.Val44=
|
|
ENST00000684530.1:c.132T>C
|
ENSP00000507439.1:p.Val44=
|
|
ENST00000684652.1:n.1872T>C
|
|
|
ENST00000340941.11:c.870T>C
MANE Select
|
ENSP00000343657.6:p.Val290=
|
|
ENST00000340941.10:c.870T>C
|
ENSP00000343657.6:p.Val290=
|
|
ENST00000505435.3:n.221T>C
|
|
|
ENST00000505787.7:n.684T>C
|
|
|
ENST00000509358.6:c.870T>C
|
ENSP00000420994.2:p.Val290=
|
|
ENST00000509539.2:c.195T>C
|
ENSP00000425474.2:p.Val65=
|
|
ENST00000510895.6:n.484T>C
|
|
|
ENST00000512218.6:c.756T>C
|
ENSP00000423202.2:p.Val252=
|
|
ENST00000629193.2:c.756T>C
|
ENSP00000486535.1:p.Val252=
|
|
NM_022132.4:c.870T>C
|
NP_071415.1:p.Val290=
|
|
XM_005248567.1:c.756T>C
|
XP_005248624.1:p.Val252=
|
|
XM_011543528.1:c.870T>C
|
XP_011541830.1:p.Val290=
|
|
XM_011543529.1:c.870T>C
|
XP_011541831.1:p.Val290=
|
|
NM_001363147.1:c.756T>C
|
NP_001350076.1:p.Val252=
|
|
XM_011543529.2:c.870T>C
|
XP_011541831.1:p.Val290=
|
|
XM_017009688.1:c.870T>C
|
XP_016865177.1:p.Val290=
|
|
XR_001742172.1:n.910T>C
|
|
|
NM_022132.5:c.870T>C
MANE Select
|
NP_071415.1:p.Val290=
|
|