|
ENST00000346169.7:c.3513G>T
(EIF4G1)
MANE Select
|
ENSP00000316879.5:p.Gly1171=
|
|
|
ENST00000435046.7:c.3447G>T
(EIF4G1)
|
ENSP00000404754.3:p.Gly1149=
|
|
|
ENST00000676453.1:c.2860G>T
(EIF4G1)
|
ENSP00000501695.1:n.2860G>T
|
|
|
ENST00000319274.10:c.2918G>T
(EIF4G1)
|
ENSP00000323737.7:p.Gly973Val
|
|
|
ENST00000342981.8:c.3516G>T
(EIF4G1)
|
ENSP00000343450.4:p.Gly1172=
|
|
|
ENST00000346169.6:c.3513G>T
(EIF4G1)
|
ENSP00000316879.4:p.Gly1171=
|
|
|
ENST00000350481.9:c.3021G>T
(EIF4G1)
|
ENSP00000317600.8:p.Gly1007=
|
|
|
ENST00000352767.7:c.3534G>T
(EIF4G1)
|
ENSP00000338020.4:p.Gly1178=
|
|
|
ENST00000382330.7:c.3534G>T
(EIF4G1)
|
ENSP00000371767.3:p.Gly1178=
|
|
|
ENST00000392537.6:c.3252G>T
(EIF4G1)
|
ENSP00000376320.2:p.Gly1084=
|
|
|
ENST00000411531.5:c.3396G>T
(EIF4G1)
|
ENSP00000395974.1:p.Gly1132=
|
|
|
ENST00000414031.5:c.3393G>T
(EIF4G1)
|
ENSP00000391935.1:p.Gly1131=
|
|
|
ENST00000424196.5:c.3534G>T
(EIF4G1)
|
ENSP00000416255.1:p.Gly1178=
|
|
|
ENST00000427845.5:c.3255G>T
(EIF4G1)
|
ENSP00000407682.1:p.Gly1085=
|
|
|
ENST00000434061.6:c.2928G>T
(EIF4G1)
|
ENSP00000411826.2:p.Gly976=
|
|
|
ENST00000435046.6:c.2925G>T
(EIF4G1)
|
ENSP00000404754.2:p.Gly975=
|
|
|
ENST00000441154.5:c.3024G>T
(EIF4G1)
|
ENSP00000399858.1:p.Gly1008=
|
|
|
ENST00000442406.5:c.*2952G>T
(EIF4G1)
|
ENSP00000400351.1:n.*2952G>T
|
|
|
ENST00000444495.1:c.2106+182593G>T
(EIF2B5)
|
ENSP00000409142.1:n.2106+182593G>T
|
|
|
ENST00000448284.1:c.674G>T
(EIF4G1)
|
|
|
|
ENST00000482303.1:n.15G>T
(EIF4G1)
|
|
|
|
NM_001194946.1:c.3534G>T
(EIF4G1)
|
NP_001181875.1:p.Gly1178=
|
|
|
NM_001194947.1:c.3534G>T
(EIF4G1)
|
NP_001181876.1:p.Gly1178=
|
|
|
NM_001291157.1:c.3393G>T
(EIF4G1)
|
NP_001278086.1:p.Gly1131=
|
|
|
NM_004953.4:c.2928G>T
(EIF4G1)
|
NP_004944.3:p.Gly976=
|
|
|
NM_182917.4:c.3516G>T
(EIF4G1)
|
NP_886553.3:p.Gly1172=
|
|
|
NM_198241.2:c.3513G>T
(EIF4G1)
|
NP_937884.1:p.Gly1171=
|
|
|
NM_198242.2:c.3021G>T
(EIF4G1)
|
NP_937885.1:p.Gly1007=
|
|
|
NM_198244.2:c.3252G>T
(EIF4G1)
|
NP_937887.1:p.Gly1084=
|
|
|
NM_001194946.2:c.3534G>T
(EIF4G1)
|
NP_001181875.2:p.Gly1178=
|
|
|
NM_001291157.2:c.3393G>T
(EIF4G1)
|
NP_001278086.2:p.Gly1131=
|
|
|
NM_004953.5:c.2928G>T
(EIF4G1)
|
NP_004944.3:p.Gly976=
|
|
|
NM_198241.3:c.3513G>T
(EIF4G1)
MANE Select
|
NP_937884.2:p.Gly1171=
|
|
|
NM_198242.3:c.3021G>T
(EIF4G1)
|
NP_937885.1:p.Gly1007=
|
|
|
NM_198244.3:c.3252G>T
(EIF4G1)
|
NP_937887.2:p.Gly1084=
|
|
|
NM_001194947.2:c.3534G>T
(EIF4G1)
|
NP_001181876.2:p.Gly1178=
|
|
