ENST00000347454.9:c.1318A>G
(EIF2B4)
MANE Select
|
ENSP00000233552.6:p.Thr440Ala
|
|
ENST00000347454.8:c.1318A>G
(EIF2B4)
|
ENSP00000233552.5:p.Thr440Ala
|
|
ENST00000405940.6:c.*584A>G
(EIF2B4)
|
ENSP00000384375.2:n.*584A>G
|
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ENST00000445933.6:c.1315A>G
(EIF2B4)
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ENSP00000394397.2:p.Thr439Ala
|
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ENST00000451130.6:c.1378A>G
(EIF2B4)
|
ENSP00000394869.2:p.Thr460Ala
|
|
ENST00000478311.1:n.311A>G
(EIF2B4)
|
|
|
ENST00000493344.6:c.1381A>G
(EIF2B4)
|
ENSP00000429323.1:p.Thr461Ala
|
|
ENST00000616081.4:c.1309A>G
(EIF2B4)
|
ENSP00000477710.1:p.Thr437Ala
|
|
ENST00000622434.4:c.*584A>G
(EIF2B4)
|
ENSP00000479991.1:n.*584A>G
|
|
NM_001034116.1:c.1318A>G
(EIF2B4)
|
NP_001029288.1:p.Thr440Ala
|
|
NM_015636.3:c.1315A>G
(EIF2B4)
|
NP_056451.3:p.Thr439Ala
|
|
NM_172195.3:c.1378A>G
(EIF2B4)
|
NP_751945.2:p.Thr460Ala
|
|
XM_005264632.1:c.1273A>G
(EIF2B4)
|
XP_005264689.1:p.Thr425Ala
|
|
XM_006712132.1:c.1270A>G
(EIF2B4)
|
XP_006712195.1:p.Thr424Ala
|
|
XM_011533147.1:c.700A>G
(EIF2B4)
|
XP_011531449.1:p.Thr234Ala
|
|
XR_939868.1:n.1772-2652T>C
(GTF3C2-AS2)
|
|
|
NM_001318965.1:c.1381A>G
(EIF2B4)
|
NP_001305894.1:p.Thr461Ala
|
|
NM_001318966.1:c.1273A>G
(EIF2B4)
|
NP_001305895.1:p.Thr425Ala
|
|
NM_001318967.1:c.1225A>G
(EIF2B4)
|
NP_001305896.1:p.Thr409Ala
|
|
NM_001318968.1:c.733A>G
(EIF2B4)
|
NP_001305897.1:p.Thr245Ala
|
|
NM_001318969.1:c.700A>G
(EIF2B4)
|
NP_001305898.1:p.Thr234Ala
|
|
XM_011533147.2:c.700A>G
(EIF2B4)
|
XP_011531449.1:p.Thr234Ala
|
|
NM_001034116.2:c.1318A>G
(EIF2B4)
MANE Select
|
NP_001029288.1:p.Thr440Ala
|
|
NM_001318965.2:c.1381A>G
(EIF2B4)
|
NP_001305894.1:p.Thr461Ala
|
|
NM_001318966.2:c.1273A>G
(EIF2B4)
|
NP_001305895.1:p.Thr425Ala
|
|
NM_001318967.2:c.1225A>G
(EIF2B4)
|
NP_001305896.1:p.Thr409Ala
|
|
NM_001318968.2:c.733A>G
(EIF2B4)
|
NP_001305897.1:p.Thr245Ala
|
|
NM_001318969.2:c.700A>G
(EIF2B4)
|
NP_001305898.1:p.Thr234Ala
|
|
NM_015636.4:c.1315A>G
(EIF2B4)
|
NP_056451.3:p.Thr439Ala
|
|
NM_172195.4:c.1378A>G
(EIF2B4)
|
NP_751945.2:p.Thr460Ala
|
|