|
ENST00000347454.9:c.1263A>T
(EIF2B4)
MANE Select
|
ENSP00000233552.6:p.Ala421=
|
|
|
ENST00000347454.8:c.1263A>T
(EIF2B4)
|
ENSP00000233552.5:p.Ala421=
|
|
|
ENST00000405940.6:c.*529A>T
(EIF2B4)
|
ENSP00000384375.2:n.*529A>T
|
|
|
ENST00000445933.6:c.1260A>T
(EIF2B4)
|
ENSP00000394397.2:p.Ala420=
|
|
|
ENST00000451130.6:c.1323A>T
(EIF2B4)
|
ENSP00000394869.2:p.Ala441=
|
|
|
ENST00000478311.1:n.256A>T
(EIF2B4)
|
|
|
|
ENST00000493344.6:c.1326A>T
(EIF2B4)
|
ENSP00000429323.1:p.Ala442=
|
|
|
ENST00000616081.4:c.1254A>T
(EIF2B4)
|
ENSP00000477710.1:p.Ala418=
|
|
|
ENST00000622434.4:c.*529A>T
(EIF2B4)
|
ENSP00000479991.1:n.*529A>T
|
|
|
NM_001034116.1:c.1263A>T
(EIF2B4)
|
NP_001029288.1:p.Ala421=
|
|
|
NM_015636.3:c.1260A>T
(EIF2B4)
|
NP_056451.3:p.Ala420=
|
|
|
NM_172195.3:c.1323A>T
(EIF2B4)
|
NP_751945.2:p.Ala441=
|
|
|
XM_005264632.1:c.1218A>T
(EIF2B4)
|
XP_005264689.1:p.Ala406=
|
|
|
XM_006712132.1:c.1215A>T
(EIF2B4)
|
XP_006712195.1:p.Ala405=
|
|
|
XM_011533147.1:c.645A>T
(EIF2B4)
|
XP_011531449.1:p.Ala215=
|
|
|
XR_939868.1:n.1772-2597T>A
(GTF3C2-AS2)
|
|
|
|
NM_001318965.1:c.1326A>T
(EIF2B4)
|
NP_001305894.1:p.Ala442=
|
|
|
NM_001318966.1:c.1218A>T
(EIF2B4)
|
NP_001305895.1:p.Ala406=
|
|
|
NM_001318967.1:c.1170A>T
(EIF2B4)
|
NP_001305896.1:p.Ala390=
|
|
|
NM_001318968.1:c.678A>T
(EIF2B4)
|
NP_001305897.1:p.Ala226=
|
|
|
NM_001318969.1:c.645A>T
(EIF2B4)
|
NP_001305898.1:p.Ala215=
|
|
|
XM_011533147.2:c.645A>T
(EIF2B4)
|
XP_011531449.1:p.Ala215=
|
|
|
NM_001034116.2:c.1263A>T
(EIF2B4)
MANE Select
|
NP_001029288.1:p.Ala421=
|
|
|
NM_001318965.2:c.1326A>T
(EIF2B4)
|
NP_001305894.1:p.Ala442=
|
|
|
NM_001318966.2:c.1218A>T
(EIF2B4)
|
NP_001305895.1:p.Ala406=
|
|
|
NM_001318967.2:c.1170A>T
(EIF2B4)
|
NP_001305896.1:p.Ala390=
|
|
|
NM_001318968.2:c.678A>T
(EIF2B4)
|
NP_001305897.1:p.Ala226=
|
|
|
NM_001318969.2:c.645A>T
(EIF2B4)
|
NP_001305898.1:p.Ala215=
|
|
|
NM_015636.4:c.1260A>T
(EIF2B4)
|
NP_056451.3:p.Ala420=
|
|
|
NM_172195.4:c.1323A>T
(EIF2B4)
|
NP_751945.2:p.Ala441=
|
|
