ENST00000346169.7:c.3535A>G
(EIF4G1)
MANE Select
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ENSP00000316879.5:p.Thr1179Ala
|
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ENST00000435046.7:c.3469A>G
(EIF4G1)
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ENSP00000404754.3:p.Thr1157Ala
|
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ENST00000676453.1:c.2882A>G
(EIF4G1)
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ENSP00000501695.1:n.2882A>G
|
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ENST00000319274.10:c.2938A>G
(EIF4G1)
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ENSP00000323737.7:p.Thr980Ala
|
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ENST00000342981.8:c.3538A>G
(EIF4G1)
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ENSP00000343450.4:p.Thr1180Ala
|
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ENST00000346169.6:c.3535A>G
(EIF4G1)
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ENSP00000316879.4:p.Thr1179Ala
|
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ENST00000350481.9:c.3043A>G
(EIF4G1)
|
ENSP00000317600.8:p.Thr1015Ala
|
|
ENST00000352767.7:c.3556A>G
(EIF4G1)
|
ENSP00000338020.4:p.Thr1186Ala
|
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ENST00000382330.7:c.3556A>G
(EIF4G1)
|
ENSP00000371767.3:p.Thr1186Ala
|
|
ENST00000392537.6:c.3274A>G
(EIF4G1)
|
ENSP00000376320.2:p.Thr1092Ala
|
|
ENST00000411531.5:c.3418A>G
(EIF4G1)
|
ENSP00000395974.1:p.Thr1140Ala
|
|
ENST00000414031.5:c.3415A>G
(EIF4G1)
|
ENSP00000391935.1:p.Thr1139Ala
|
|
ENST00000424196.5:c.3556A>G
(EIF4G1)
|
ENSP00000416255.1:p.Thr1186Ala
|
|
ENST00000427845.5:c.3277A>G
(EIF4G1)
|
ENSP00000407682.1:p.Thr1093Ala
|
|
ENST00000434061.6:c.2950A>G
(EIF4G1)
|
ENSP00000411826.2:p.Thr984Ala
|
|
ENST00000435046.6:c.2947A>G
(EIF4G1)
|
ENSP00000404754.2:p.Thr983Ala
|
|
ENST00000441154.5:c.3046A>G
(EIF4G1)
|
ENSP00000399858.1:p.Thr1016Ala
|
|
ENST00000442406.5:c.*2974A>G
(EIF4G1)
|
ENSP00000400351.1:n.*2974A>G
|
|
ENST00000444495.1:c.2106+182615A>G
(EIF2B5)
|
ENSP00000409142.1:n.2106+182615A>G
|
|
ENST00000482303.1:n.37A>G
(EIF4G1)
|
|
|
NM_001194946.1:c.3556A>G
(EIF4G1)
|
NP_001181875.1:p.Thr1186Ala
|
|
NM_001194947.1:c.3556A>G
(EIF4G1)
|
NP_001181876.1:p.Thr1186Ala
|
|
NM_001291157.1:c.3415A>G
(EIF4G1)
|
NP_001278086.1:p.Thr1139Ala
|
|
NM_004953.4:c.2950A>G
(EIF4G1)
|
NP_004944.3:p.Thr984Ala
|
|
NM_182917.4:c.3538A>G
(EIF4G1)
|
NP_886553.3:p.Thr1180Ala
|
|
NM_198241.2:c.3535A>G
(EIF4G1)
|
NP_937884.1:p.Thr1179Ala
|
|
NM_198242.2:c.3043A>G
(EIF4G1)
|
NP_937885.1:p.Thr1015Ala
|
|
NM_198244.2:c.3274A>G
(EIF4G1)
|
NP_937887.1:p.Thr1092Ala
|
|
NM_001194946.2:c.3556A>G
(EIF4G1)
|
NP_001181875.2:p.Thr1186Ala
|
|
NM_001291157.2:c.3415A>G
(EIF4G1)
|
NP_001278086.2:p.Thr1139Ala
|
|
NM_004953.5:c.2950A>G
(EIF4G1)
|
NP_004944.3:p.Thr984Ala
|
|
NM_198241.3:c.3535A>G
(EIF4G1)
MANE Select
|
NP_937884.2:p.Thr1179Ala
|
|
NM_198242.3:c.3043A>G
(EIF4G1)
|
NP_937885.1:p.Thr1015Ala
|
|
NM_198244.3:c.3274A>G
(EIF4G1)
|
NP_937887.2:p.Thr1092Ala
|
|
NM_001194947.2:c.3556A>G
(EIF4G1)
|
NP_001181876.2:p.Thr1186Ala
|
|