|
ENST00000505435.4:n.920G=
|
|
|
|
ENST00000505787.8:n.2804G=
|
|
|
|
ENST00000509358.7:c.964G=
|
ENSP00000420994.3:p.Gly322=
|
|
|
ENST00000509539.3:c.226G=
|
ENSP00000425474.3:p.Gly76=
|
|
|
ENST00000510895.7:n.1087G=
|
|
|
|
ENST00000629193.3:c.850G=
|
ENSP00000486535.2:p.Gly284=
|
|
|
ENST00000681968.1:c.457G=
|
ENSP00000508143.1:p.Gly153=
|
|
|
ENST00000682045.1:c.820G=
|
ENSP00000507329.1:p.Gly274=
|
|
|
ENST00000682214.1:c.571G=
|
ENSP00000507336.1:p.Gly191=
|
|
|
ENST00000682499.1:n.1785G=
|
|
|
|
ENST00000682541.1:c.964G=
|
ENSP00000507673.1:p.Gly322=
|
|
|
ENST00000682687.1:c.964G=
|
ENSP00000507945.1:p.Gly322=
|
|
|
ENST00000682727.1:c.964G=
|
ENSP00000507393.1:p.Gly322=
|
|
|
ENST00000682876.1:c.1093G=
|
ENSP00000508389.1:p.Gly365=
|
|
|
ENST00000683098.1:c.803+3026G=
|
ENSP00000507670.1:n.803+3026G=
|
|
|
ENST00000683258.1:c.*685G=
|
ENSP00000507448.1:n.*685G=
|
|
|
ENST00000683339.1:c.748G=
|
ENSP00000507758.1:p.Gly250=
|
|
|
ENST00000683403.1:c.874G=
|
ENSP00000507896.1:p.Gly292=
|
|
|
ENST00000683429.1:c.571G=
|
ENSP00000507697.1:p.Gly191=
|
|
|
ENST00000683665.1:c.964G=
|
ENSP00000507068.1:p.Gly322=
|
|
|
ENST00000683789.1:c.850G=
|
ENSP00000507012.1:p.Gly284=
|
|
|
ENST00000683847.1:n.808G=
|
|
|
|
ENST00000683882.1:c.964G=
|
ENSP00000506735.1:p.Gly322=
|
|
|
ENST00000684024.1:c.*635G=
|
ENSP00000507175.1:n.*635G=
|
|
|
ENST00000684254.1:c.*690G=
|
ENSP00000508001.1:n.*690G=
|
|
|
ENST00000684310.1:c.165+169G=
|
ENSP00000507550.1:n.165+169G=
|
|
|
ENST00000684530.1:c.226G=
|
ENSP00000507439.1:p.Gly76=
|
|
|
ENST00000684652.1:n.1966G=
|
|
|
|
ENST00000340941.11:c.964G=
MANE Select
|
ENSP00000343657.6:p.Gly322=
|
|
|
ENST00000340941.10:c.964G=
|
ENSP00000343657.6:p.Gly322=
|
|
|
ENST00000505435.3:n.315G=
|
|
|
|
ENST00000509358.6:c.964G=
|
ENSP00000420994.2:p.Gly322=
|
|
|
ENST00000509539.2:c.289G=
|
ENSP00000425474.2:p.Gly97=
|
|
|
ENST00000510895.6:n.578G=
|
|
|
|
ENST00000512218.6:c.850G=
|
ENSP00000423202.2:p.Gly284=
|
|
|
ENST00000629193.2:c.850G=
|
ENSP00000486535.1:p.Gly284=
|
|
|
NM_022132.4:c.964G=
|
NP_071415.1:p.Gly322=
|
|
|
XM_005248567.1:c.850G=
|
XP_005248624.1:p.Gly284=
|
|
|
XM_011543528.1:c.964G=
|
XP_011541830.1:p.Gly322=
|
|
|
XM_011543529.1:c.964G=
|
XP_011541831.1:p.Gly322=
|
|
|
NM_001363147.1:c.850G=
|
NP_001350076.1:p.Gly284=
|
|
|
XM_011543529.2:c.964G=
|
XP_011541831.1:p.Gly322=
|
|
|
XM_017009688.1:c.964G=
|
XP_016865177.1:p.Gly322=
|
|
|
XR_001742172.1:n.1004G=
|
|
|
|
NM_022132.5:c.964G=
MANE Select
|
NP_071415.1:p.Gly322=
|
|
