ENST00000713569.1:c.1682G>T
(DLAT)
|
ENSP00000518862.1:p.Gly561Val
|
|
ENST00000280346.11:c.1682G>T
(DLAT)
MANE Select
|
ENSP00000280346.7:p.Gly561Val
|
|
ENST00000527231.2:n.1729G>T
(DLAT)
|
|
|
ENST00000531306.2:c.1301G>T
(DLAT)
|
ENSP00000433432.2:p.Gly434Val
|
|
ENST00000679368.1:c.*609G>T
(DLAT)
|
ENSP00000505314.1:n.*609G>T
|
|
ENST00000679614.1:c.1079G>T
(DLAT)
|
ENSP00000506007.1:p.Gly360Val
|
|
ENST00000679815.1:c.*1115G>T
(DLAT)
|
ENSP00000504880.1:n.*1115G>T
|
|
ENST00000679878.1:c.1649G>T
(DLAT)
|
ENSP00000505567.1:p.Gly550Val
|
|
ENST00000680010.1:c.*823G>T
(DLAT)
|
ENSP00000505768.1:n.*823G>T
|
|
ENST00000680154.1:n.1013G>T
(DLAT)
|
|
|
ENST00000680331.1:c.1403G>T
(DLAT)
|
ENSP00000506707.1:p.Gly468Val
|
|
ENST00000680411.1:c.1427G>T
(DLAT)
|
ENSP00000505915.1:p.Gly476Val
|
|
ENST00000681316.1:c.1676G>T
(DLAT)
|
ENSP00000506560.1:p.Gly559Val
|
|
ENST00000681328.1:c.1661G>T
(DLAT)
|
ENSP00000506355.1:p.Gly554Val
|
|
ENST00000681339.1:c.1574G>T
(DLAT)
|
ENSP00000506167.1:p.Gly525Val
|
|
ENST00000681638.1:c.*1035G>T
(DLAT)
|
ENSP00000506090.1:n.*1035G>T
|
|
ENST00000280346.10:c.1682G>T
(DLAT)
|
ENSP00000280346.6:p.Gly561Val
|
|
ENST00000393051.5:c.1367G>T
(DLAT)
|
ENSP00000376771.1:p.Gly456Val
|
|
ENST00000527231.1:n.76G>T
(DLAT)
|
|
|
ENST00000531306.1:c.1178G>T
(DLAT)
|
ENSP00000433432.1:p.Gly393Val
|
|
ENST00000533297.1:c.*1357G>T
(DLAT)
|
ENSP00000435374.1:n.*1357G>T
|
|
NM_001931.4:c.1682G>T
(DLAT)
|
NP_001922.2:p.Gly561Val
|
|
XM_011542590.1:c.814-248C>A
(PIH1D2)
|
XP_011540892.1:n.814-248C>A
|
|
XM_011542592.1:c.814-8355C>A
(PIH1D2)
|
XP_011540894.1:n.814-8355C>A
|
|
XM_011542647.1:c.1574G>T
(DLAT)
|
XP_011540949.1:p.Gly525Val
|
|
XM_011542647.3:c.1574G>T
(DLAT)
|
XP_011540949.1:p.Gly525Val
|
|
XM_017017202.2:c.814-5262C>A
(PIH1D2)
|
XP_016872691.1:n.814-5262C>A
|
|
XM_017017203.2:c.814-248C>A
(PIH1D2)
|
XP_016872692.1:n.814-248C>A
|
|
XM_017017204.2:c.814-5291C>A
(PIH1D2)
|
XP_016872693.1:n.814-5291C>A
|
|
XM_017017205.2:c.814-8355C>A
(PIH1D2)
|
XP_016872694.1:n.814-8355C>A
|
|
NM_001372031.1:c.1700G>T
(DLAT)
|
NP_001358960.1:p.Gly567Val
|
|
NM_001372032.1:c.1676G>T
(DLAT)
|
NP_001358961.1:p.Gly559Val
|
|
NM_001372033.1:c.1661G>T
(DLAT)
|
NP_001358962.1:p.Gly554Val
|
|
NM_001372034.1:c.1649G>T
(DLAT)
|
NP_001358963.1:p.Gly550Val
|
|
NM_001372035.1:c.1574G>T
(DLAT)
|
NP_001358964.1:p.Gly525Val
|
|
NM_001372036.1:c.1556G>T
(DLAT)
|
NP_001358965.1:p.Gly519Val
|
|
NM_001372037.1:c.1514G>T
(DLAT)
|
NP_001358966.1:p.Gly505Val
|
|
NM_001372038.1:c.1403G>T
(DLAT)
|
NP_001358967.1:p.Gly468Val
|
|
NM_001372039.1:c.1367G>T
(DLAT)
|
NP_001358968.1:p.Gly456Val
|
|
NM_001372040.1:c.1301G>T
(DLAT)
|
NP_001358969.1:p.Gly434Val
|
|
NM_001372041.1:c.1259G>T
(DLAT)
|
NP_001358970.1:p.Gly420Val
|
|
NM_001372042.1:c.1220G>T
(DLAT)
|
NP_001358971.1:p.Gly407Val
|
|
NM_001931.5:c.1682G>T
(DLAT)
MANE Select
|
NP_001922.2:p.Gly561Val
|
|
NR_164072.1:n.1559G>T
(DLAT)
|
|
|