ENST00000347454.9:c.1335G>A
(EIF2B4)
MANE Select
|
ENSP00000233552.6:p.Glu445=
|
|
ENST00000347454.8:c.1335G>A
(EIF2B4)
|
ENSP00000233552.5:p.Glu445=
|
|
ENST00000405940.6:c.*601G>A
(EIF2B4)
|
ENSP00000384375.2:n.*601G>A
|
|
ENST00000445933.6:c.1332G>A
(EIF2B4)
|
ENSP00000394397.2:p.Glu444=
|
|
ENST00000451130.6:c.1395G>A
(EIF2B4)
|
ENSP00000394869.2:p.Glu465=
|
|
ENST00000478311.1:n.328G>A
(EIF2B4)
|
|
|
ENST00000493344.6:c.1398G>A
(EIF2B4)
|
ENSP00000429323.1:p.Glu466=
|
|
ENST00000616081.4:c.1326G>A
(EIF2B4)
|
ENSP00000477710.1:p.Glu442=
|
|
ENST00000622434.4:c.*601G>A
(EIF2B4)
|
ENSP00000479991.1:n.*601G>A
|
|
NM_001034116.1:c.1335G>A
(EIF2B4)
|
NP_001029288.1:p.Glu445=
|
|
NM_015636.3:c.1332G>A
(EIF2B4)
|
NP_056451.3:p.Glu444=
|
|
NM_172195.3:c.1395G>A
(EIF2B4)
|
NP_751945.2:p.Glu465=
|
|
XM_005264632.1:c.1290G>A
(EIF2B4)
|
XP_005264689.1:p.Glu430=
|
|
XM_006712132.1:c.1287G>A
(EIF2B4)
|
XP_006712195.1:p.Glu429=
|
|
XM_011533147.1:c.717G>A
(EIF2B4)
|
XP_011531449.1:p.Glu239=
|
|
XR_939868.1:n.1772-2669C>T
(GTF3C2-AS2)
|
|
|
NM_001318965.1:c.1398G>A
(EIF2B4)
|
NP_001305894.1:p.Glu466=
|
|
NM_001318966.1:c.1290G>A
(EIF2B4)
|
NP_001305895.1:p.Glu430=
|
|
NM_001318967.1:c.1242G>A
(EIF2B4)
|
NP_001305896.1:p.Glu414=
|
|
NM_001318968.1:c.750G>A
(EIF2B4)
|
NP_001305897.1:p.Glu250=
|
|
NM_001318969.1:c.717G>A
(EIF2B4)
|
NP_001305898.1:p.Glu239=
|
|
XM_011533147.2:c.717G>A
(EIF2B4)
|
XP_011531449.1:p.Glu239=
|
|
NM_001034116.2:c.1335G>A
(EIF2B4)
MANE Select
|
NP_001029288.1:p.Glu445=
|
|
NM_001318965.2:c.1398G>A
(EIF2B4)
|
NP_001305894.1:p.Glu466=
|
|
NM_001318966.2:c.1290G>A
(EIF2B4)
|
NP_001305895.1:p.Glu430=
|
|
NM_001318967.2:c.1242G>A
(EIF2B4)
|
NP_001305896.1:p.Glu414=
|
|
NM_001318968.2:c.750G>A
(EIF2B4)
|
NP_001305897.1:p.Glu250=
|
|
NM_001318969.2:c.717G>A
(EIF2B4)
|
NP_001305898.1:p.Glu239=
|
|
NM_015636.4:c.1332G>A
(EIF2B4)
|
NP_056451.3:p.Glu444=
|
|
NM_172195.4:c.1395G>A
(EIF2B4)
|
NP_751945.2:p.Glu465=
|
|