ENST00000269571.10:c.3576G>C
MANE Select
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ENSP00000269571.4:p.Glu1192Asp
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ENST00000269571.9:c.3576G>C
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ENSP00000269571.4:p.Glu1192Asp
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ENST00000406381.6:c.3486G>C
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ENSP00000385185.2:p.Glu1162Asp
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ENST00000445658.6:c.2748G>C
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ENSP00000404047.2:p.Glu916Asp
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ENST00000541774.5:c.3531G>C
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ENSP00000446466.1:p.Glu1177Asp
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ENST00000578373.5:c.*3366G>C
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ENSP00000463427.1:n.*3366G>C
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ENST00000584450.5:c.*155G>C
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ENSP00000463714.1:n.*155G>C
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ENST00000584601.5:c.3486G>C
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ENSP00000462438.1:p.Glu1162Asp
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NM_001005862.2:c.3486G>C , LRG_724t1:c.3486G>C
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NP_001005862.1:p.Glu1162Asp
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NM_001289936.1:c.3531G>C , LRG_724t4:c.3531G>C
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NP_001276865.1:p.Glu1177Asp
|
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NM_001289937.1:c.*155G>C
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NP_001276866.1:n.*155G>C
|
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NM_004448.3:c.3576G>C , LRG_724t2:c.3576G>C
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NP_004439.2:p.Glu1192Asp
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NR_110535.1:n.3900G>C
|
|
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XM_024450641.1:c.3714G>C
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XP_024306409.1:p.Glu1238Asp
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XM_024450642.1:c.3669G>C
|
XP_024306410.1:p.Glu1223Asp
|
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XM_024450643.1:c.3624G>C
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XP_024306411.1:p.Glu1208Asp
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NM_001005862.3:c.3486G>C
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NP_001005862.1:p.Glu1162Asp
|
|
NM_001289936.2:c.3531G>C
|
NP_001276865.1:p.Glu1177Asp
|
|
NM_001289937.2:c.*155G>C
|
NP_001276866.1:n.*155G>C
|
|
NM_001382782.1:c.3486G>C
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NP_001369711.1:p.Glu1162Asp
|
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NM_001382783.1:c.3486G>C
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NP_001369712.1:p.Glu1162Asp
|
|
NM_001382784.1:c.3693G>C
|
NP_001369713.1:p.Glu1231Asp
|
|
NM_001382785.1:c.3678G>C
|
NP_001369714.1:p.Glu1226Asp
|
|
NM_001382786.1:c.3657G>C
|
NP_001369715.1:p.Glu1219Asp
|
|
NM_001382787.1:c.3651G>C
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NP_001369716.1:p.Glu1217Asp
|
|
NM_001382788.1:c.3606G>C
|
NP_001369717.1:p.Glu1202Asp
|
|
NM_001382789.1:c.3597G>C
|
NP_001369718.1:p.Glu1199Asp
|
|
NM_001382790.1:c.3573G>C
|
NP_001369719.1:p.Glu1191Asp
|
|
NM_001382791.1:c.3567G>C
|
NP_001369720.1:p.Glu1189Asp
|
|
NM_001382792.1:c.3540G>C
|
NP_001369721.1:p.Glu1180Asp
|
|
NM_001382793.1:c.3534G>C
|
NP_001369722.1:p.Glu1178Asp
|
|
NM_001382794.1:c.3534G>C
|
NP_001369723.1:p.Glu1178Asp
|
|
NM_001382795.1:c.3528G>C
|
NP_001369724.1:p.Glu1176Asp
|
|
NM_001382796.1:c.3489G>C
|
NP_001369725.1:p.Glu1163Asp
|
|
NM_001382797.1:c.3477G>C
|
NP_001369726.1:p.Glu1159Asp
|
|
NM_001382798.1:c.3420G>C
|
NP_001369727.1:p.Glu1140Asp
|
|
NM_001382799.1:c.3396G>C
|
NP_001369728.1:p.Glu1132Asp
|
|
NM_001382800.1:c.3390G>C
|
NP_001369729.1:p.Glu1130Asp
|
|
NM_001382801.1:c.3372G>C
|
NP_001369730.1:p.Glu1124Asp
|
|
NM_001382802.1:c.3318G>C
|
NP_001369731.1:p.Glu1106Asp
|
|
NM_001382803.1:c.*155G>C
|
NP_001369732.1:n.*155G>C
|
|
NM_001382804.1:c.2748G>C
|
NP_001369733.1:p.Glu916Asp
|
|
NM_001382805.1:c.2625G>C
|
NP_001369734.1:p.Glu875Asp
|
|
NM_001382806.1:c.2538G>C
|
NP_001369735.1:p.Glu846Asp
|
|
NM_004448.4:c.3576G>C
MANE Select
|
NP_004439.2:p.Glu1192Asp
|
|
NR_110535.2:n.3814G>C
|
|
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