|
ENST00000346169.7:c.3451G>T
(EIF4G1)
MANE Select
|
ENSP00000316879.5:p.Gly1151Cys
|
|
|
ENST00000435046.7:c.3385G>T
(EIF4G1)
|
ENSP00000404754.3:p.Gly1129Cys
|
|
|
ENST00000676453.1:c.2798G>T
(EIF4G1)
|
ENSP00000501695.1:n.2798G>T
|
|
|
ENST00000319274.10:c.2857G>T
(EIF4G1)
|
ENSP00000323737.7:p.Gly953Cys
|
|
|
ENST00000342981.8:c.3454G>T
(EIF4G1)
|
ENSP00000343450.4:p.Gly1152Cys
|
|
|
ENST00000346169.6:c.3451G>T
(EIF4G1)
|
ENSP00000316879.4:p.Gly1151Cys
|
|
|
ENST00000350481.9:c.2959G>T
(EIF4G1)
|
ENSP00000317600.8:p.Gly987Cys
|
|
|
ENST00000352767.7:c.3472G>T
(EIF4G1)
|
ENSP00000338020.4:p.Gly1158Cys
|
|
|
ENST00000382330.7:c.3472G>T
(EIF4G1)
|
ENSP00000371767.3:p.Gly1158Cys
|
|
|
ENST00000392537.6:c.3190G>T
(EIF4G1)
|
ENSP00000376320.2:p.Gly1064Cys
|
|
|
ENST00000411531.5:c.3334G>T
(EIF4G1)
|
ENSP00000395974.1:p.Gly1112Cys
|
|
|
ENST00000414031.5:c.3331G>T
(EIF4G1)
|
ENSP00000391935.1:p.Gly1111Cys
|
|
|
ENST00000424196.5:c.3472G>T
(EIF4G1)
|
ENSP00000416255.1:p.Gly1158Cys
|
|
|
ENST00000427845.5:c.3193G>T
(EIF4G1)
|
ENSP00000407682.1:p.Gly1065Cys
|
|
|
ENST00000434061.6:c.2866G>T
(EIF4G1)
|
ENSP00000411826.2:p.Gly956Cys
|
|
|
ENST00000435046.6:c.2863G>T
(EIF4G1)
|
ENSP00000404754.2:p.Gly955Cys
|
|
|
ENST00000441154.5:c.2962G>T
(EIF4G1)
|
ENSP00000399858.1:p.Gly988Cys
|
|
|
ENST00000442406.5:c.*2890G>T
(EIF4G1)
|
ENSP00000400351.1:n.*2890G>T
|
|
|
ENST00000444495.1:c.2106+182531G>T
(EIF2B5)
|
ENSP00000409142.1:n.2106+182531G>T
|
|
|
ENST00000448284.1:c.612G>T
(EIF4G1)
|
|
|
|
NM_001194946.1:c.3472G>T
(EIF4G1)
|
NP_001181875.1:p.Gly1158Cys
|
|
|
NM_001194947.1:c.3472G>T
(EIF4G1)
|
NP_001181876.1:p.Gly1158Cys
|
|
|
NM_001291157.1:c.3331G>T
(EIF4G1)
|
NP_001278086.1:p.Gly1111Cys
|
|
|
NM_004953.4:c.2866G>T
(EIF4G1)
|
NP_004944.3:p.Gly956Cys
|
|
|
NM_182917.4:c.3454G>T
(EIF4G1)
|
NP_886553.3:p.Gly1152Cys
|
|
|
NM_198241.2:c.3451G>T
(EIF4G1)
|
NP_937884.1:p.Gly1151Cys
|
|
|
NM_198242.2:c.2959G>T
(EIF4G1)
|
NP_937885.1:p.Gly987Cys
|
|
|
NM_198244.2:c.3190G>T
(EIF4G1)
|
NP_937887.1:p.Gly1064Cys
|
|
|
NM_001194946.2:c.3472G>T
(EIF4G1)
|
NP_001181875.2:p.Gly1158Cys
|
|
|
NM_001291157.2:c.3331G>T
(EIF4G1)
|
NP_001278086.2:p.Gly1111Cys
|
|
|
NM_004953.5:c.2866G>T
(EIF4G1)
|
NP_004944.3:p.Gly956Cys
|
|
|
NM_198241.3:c.3451G>T
(EIF4G1)
MANE Select
|
NP_937884.2:p.Gly1151Cys
|
|
|
NM_198242.3:c.2959G>T
(EIF4G1)
|
NP_937885.1:p.Gly987Cys
|
|
|
NM_198244.3:c.3190G>T
(EIF4G1)
|
NP_937887.2:p.Gly1064Cys
|
|
|
NM_001194947.2:c.3472G>T
(EIF4G1)
|
NP_001181876.2:p.Gly1158Cys
|
|
