ENST00000346169.7:c.3541G>A
(EIF4G1)
MANE Select
|
ENSP00000316879.5:p.Ala1181Thr
|
|
ENST00000435046.7:c.3475G>A
(EIF4G1)
|
ENSP00000404754.3:p.Ala1159Thr
|
|
ENST00000676453.1:c.2888G>A
(EIF4G1)
|
ENSP00000501695.1:n.2888G>A
|
|
ENST00000319274.10:c.2944G>A
(EIF4G1)
|
ENSP00000323737.7:p.Ala982Thr
|
|
ENST00000342981.8:c.3544G>A
(EIF4G1)
|
ENSP00000343450.4:p.Ala1182Thr
|
|
ENST00000346169.6:c.3541G>A
(EIF4G1)
|
ENSP00000316879.4:p.Ala1181Thr
|
|
ENST00000350481.9:c.3049G>A
(EIF4G1)
|
ENSP00000317600.8:p.Ala1017Thr
|
|
ENST00000352767.7:c.3562G>A
(EIF4G1)
|
ENSP00000338020.4:p.Ala1188Thr
|
|
ENST00000382330.7:c.3562G>A
(EIF4G1)
|
ENSP00000371767.3:p.Ala1188Thr
|
|
ENST00000392537.6:c.3280G>A
(EIF4G1)
|
ENSP00000376320.2:p.Ala1094Thr
|
|
ENST00000411531.5:c.3424G>A
(EIF4G1)
|
ENSP00000395974.1:p.Ala1142Thr
|
|
ENST00000414031.5:c.3421G>A
(EIF4G1)
|
ENSP00000391935.1:p.Ala1141Thr
|
|
ENST00000424196.5:c.3562G>A
(EIF4G1)
|
ENSP00000416255.1:p.Ala1188Thr
|
|
ENST00000427845.5:c.3283G>A
(EIF4G1)
|
ENSP00000407682.1:p.Ala1095Thr
|
|
ENST00000434061.6:c.2956G>A
(EIF4G1)
|
ENSP00000411826.2:p.Ala986Thr
|
|
ENST00000435046.6:c.2953G>A
(EIF4G1)
|
ENSP00000404754.2:p.Ala985Thr
|
|
ENST00000441154.5:c.3052G>A
(EIF4G1)
|
ENSP00000399858.1:p.Ala1018Thr
|
|
ENST00000442406.5:c.*2980G>A
(EIF4G1)
|
ENSP00000400351.1:n.*2980G>A
|
|
ENST00000444495.1:c.2106+182621G>A
(EIF2B5)
|
ENSP00000409142.1:n.2106+182621G>A
|
|
ENST00000482303.1:n.43G>A
(EIF4G1)
|
|
|
NM_001194946.1:c.3562G>A
(EIF4G1)
|
NP_001181875.1:p.Ala1188Thr
|
|
NM_001194947.1:c.3562G>A
(EIF4G1)
|
NP_001181876.1:p.Ala1188Thr
|
|
NM_001291157.1:c.3421G>A
(EIF4G1)
|
NP_001278086.1:p.Ala1141Thr
|
|
NM_004953.4:c.2956G>A
(EIF4G1)
|
NP_004944.3:p.Ala986Thr
|
|
NM_182917.4:c.3544G>A
(EIF4G1)
|
NP_886553.3:p.Ala1182Thr
|
|
NM_198241.2:c.3541G>A
(EIF4G1)
|
NP_937884.1:p.Ala1181Thr
|
|
NM_198242.2:c.3049G>A
(EIF4G1)
|
NP_937885.1:p.Ala1017Thr
|
|
NM_198244.2:c.3280G>A
(EIF4G1)
|
NP_937887.1:p.Ala1094Thr
|
|
NM_001194946.2:c.3562G>A
(EIF4G1)
|
NP_001181875.2:p.Ala1188Thr
|
|
NM_001291157.2:c.3421G>A
(EIF4G1)
|
NP_001278086.2:p.Ala1141Thr
|
|
NM_004953.5:c.2956G>A
(EIF4G1)
|
NP_004944.3:p.Ala986Thr
|
|
NM_198241.3:c.3541G>A
(EIF4G1)
MANE Select
|
NP_937884.2:p.Ala1181Thr
|
|
NM_198242.3:c.3049G>A
(EIF4G1)
|
NP_937885.1:p.Ala1017Thr
|
|
NM_198244.3:c.3280G>A
(EIF4G1)
|
NP_937887.2:p.Ala1094Thr
|
|
NM_001194947.2:c.3562G>A
(EIF4G1)
|
NP_001181876.2:p.Ala1188Thr
|
|