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ENST00000505435.4:n.2761A=
|
|
|
|
ENST00000505787.8:n.2984A=
|
|
|
|
ENST00000509539.3:c.479A=
|
ENSP00000425474.3:n.479A=
|
|
|
ENST00000681968.1:c.646A=
|
ENSP00000508143.1:p.Thr216=
|
|
|
ENST00000681991.1:n.1237A=
|
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|
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ENST00000682045.1:c.1009A=
|
ENSP00000507329.1:p.Thr337=
|
|
|
ENST00000682214.1:c.760A=
|
ENSP00000507336.1:p.Thr254=
|
|
|
ENST00000682231.1:n.171A=
|
|
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ENST00000682438.1:n.3152A=
|
|
|
|
ENST00000682499.1:n.1974A=
|
|
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ENST00000682541.1:c.*51A=
|
ENSP00000507673.1:n.*51A=
|
|
|
ENST00000682640.1:n.857A=
|
|
|
|
ENST00000682667.1:n.1318A=
|
|
|
|
ENST00000682687.1:c.*105A=
|
ENSP00000507945.1:n.*105A=
|
|
|
ENST00000682727.1:c.1144A=
|
ENSP00000507393.1:p.Thr382=
|
|
|
ENST00000682876.1:c.1282A=
|
ENSP00000508389.1:p.Thr428=
|
|
|
ENST00000683098.1:c.807A=
|
ENSP00000507670.1:p.Val269=
|
|
|
ENST00000683258.1:c.*874A=
|
ENSP00000507448.1:n.*874A=
|
|
|
ENST00000683339.1:c.937A=
|
ENSP00000507758.1:p.Thr313=
|
|
|
ENST00000683403.1:c.1063A=
|
ENSP00000507896.1:p.Thr355=
|
|
|
ENST00000683429.1:c.760A=
|
ENSP00000507697.1:p.Thr254=
|
|
|
ENST00000683789.1:c.1039A=
|
ENSP00000507012.1:p.Thr347=
|
|
|
ENST00000683847.1:n.1323A=
|
|
|
|
ENST00000683882.1:c.*94A=
|
ENSP00000506735.1:n.*94A=
|
|
|
ENST00000684024.1:c.*824A=
|
ENSP00000507175.1:n.*824A=
|
|
|
ENST00000684132.1:c.81A=
|
|
|
|
ENST00000684254.1:c.*879A=
|
ENSP00000508001.1:n.*879A=
|
|
|
ENST00000684310.1:c.319A=
|
ENSP00000507550.1:p.Thr107=
|
|
|
ENST00000684474.1:n.789A=
|
|
|
|
ENST00000684530.1:c.335-2883A=
|
ENSP00000507439.1:n.335-2883A=
|
|
|
ENST00000684686.1:n.772A=
|
|
|
|
ENST00000340941.11:c.1153A=
MANE Select
|
ENSP00000343657.6:p.Thr385=
|
|
|
ENST00000340941.10:c.1153A=
|
ENSP00000343657.6:p.Thr385=
|
|
|
ENST00000509539.2:c.469A=
|
ENSP00000425474.2:p.Thr157=
|
|
|
ENST00000512218.6:c.*105A=
|
ENSP00000423202.2:n.*105A=
|
|
|
NM_022132.4:c.1153A=
|
NP_071415.1:p.Thr385=
|
|
|
XM_005248567.1:c.1039A=
|
XP_005248624.1:p.Thr347=
|
|
|
NM_001363147.1:c.1039A=
|
NP_001350076.1:p.Thr347=
|
|
|
XR_001742172.1:n.1241A=
|
|
|
|
NM_022132.5:c.1153A=
MANE Select
|
NP_071415.1:p.Thr385=
|
|
