ENST00000347454.9:c.1115C>T
(EIF2B4)
MANE Select
|
ENSP00000233552.6:p.Thr372Ile
|
|
ENST00000347454.8:c.1115C>T
(EIF2B4)
|
ENSP00000233552.5:p.Thr372Ile
|
|
ENST00000405940.6:c.*381C>T
(EIF2B4)
|
ENSP00000384375.2:n.*381C>T
|
|
ENST00000417567.1:c.689C>T
(EIF2B4)
|
|
|
ENST00000445933.6:c.1112C>T
(EIF2B4)
|
ENSP00000394397.2:p.Thr371Ile
|
|
ENST00000451130.6:c.1175C>T
(EIF2B4)
|
ENSP00000394869.2:p.Thr392Ile
|
|
ENST00000475582.5:n.3016C>T
(EIF2B4)
|
|
|
ENST00000493344.6:c.1178C>T
(EIF2B4)
|
ENSP00000429323.1:p.Thr393Ile
|
|
ENST00000616081.4:c.1106C>T
(EIF2B4)
|
ENSP00000477710.1:p.Thr369Ile
|
|
ENST00000622434.4:c.*381C>T
(EIF2B4)
|
ENSP00000479991.1:n.*381C>T
|
|
NM_001034116.1:c.1115C>T
(EIF2B4)
|
NP_001029288.1:p.Thr372Ile
|
|
NM_015636.3:c.1112C>T
(EIF2B4)
|
NP_056451.3:p.Thr371Ile
|
|
NM_172195.3:c.1175C>T
(EIF2B4)
|
NP_751945.2:p.Thr392Ile
|
|
XM_005264632.1:c.1070C>T
(EIF2B4)
|
XP_005264689.1:p.Thr357Ile
|
|
XM_006712132.1:c.1067C>T
(EIF2B4)
|
XP_006712195.1:p.Thr356Ile
|
|
XM_011533147.1:c.497C>T
(EIF2B4)
|
XP_011531449.1:p.Thr166Ile
|
|
XR_939868.1:n.1772-589G>A
(GTF3C2-AS2)
|
|
|
NM_001318965.1:c.1178C>T
(EIF2B4)
|
NP_001305894.1:p.Thr393Ile
|
|
NM_001318966.1:c.1070C>T
(EIF2B4)
|
NP_001305895.1:p.Thr357Ile
|
|
NM_001318967.1:c.1022C>T
(EIF2B4)
|
NP_001305896.1:p.Thr341Ile
|
|
NM_001318968.1:c.530C>T
(EIF2B4)
|
NP_001305897.1:p.Thr177Ile
|
|
NM_001318969.1:c.497C>T
(EIF2B4)
|
NP_001305898.1:p.Thr166Ile
|
|
XM_011533147.2:c.497C>T
(EIF2B4)
|
XP_011531449.1:p.Thr166Ile
|
|
NM_001034116.2:c.1115C>T
(EIF2B4)
MANE Select
|
NP_001029288.1:p.Thr372Ile
|
|
NM_001318965.2:c.1178C>T
(EIF2B4)
|
NP_001305894.1:p.Thr393Ile
|
|
NM_001318966.2:c.1070C>T
(EIF2B4)
|
NP_001305895.1:p.Thr357Ile
|
|
NM_001318967.2:c.1022C>T
(EIF2B4)
|
NP_001305896.1:p.Thr341Ile
|
|
NM_001318968.2:c.530C>T
(EIF2B4)
|
NP_001305897.1:p.Thr177Ile
|
|
NM_001318969.2:c.497C>T
(EIF2B4)
|
NP_001305898.1:p.Thr166Ile
|
|
NM_015636.4:c.1112C>T
(EIF2B4)
|
NP_056451.3:p.Thr371Ile
|
|
NM_172195.4:c.1175C>T
(EIF2B4)
|
NP_751945.2:p.Thr392Ile
|
|