ENST00000470094.2:c.*599A>C
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ENSP00000434898.2:n.*599A>C
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ENST00000528762.2:c.*1443A>C
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ENSP00000433168.2:n.*1443A>C
|
|
ENST00000530893.7:c.9707A>C
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ENSP00000499438.2:p.Glu3236Ala
|
|
ENST00000665585.2:c.*1638A>C
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ENSP00000499570.2:n.*1638A>C
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ENST00000700202.2:c.10025A>C
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ENSP00000514856.2:p.Glu3342Ala
|
|
ENST00000700202.1:c.2492A>C
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ENSP00000514856.1:p.Glu831Ala
|
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ENST00000700203.1:n.2203A>C
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|
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ENST00000380152.8:c.10076A>C
MANE Select
|
ENSP00000369497.3:p.Glu3359Ala
|
|
ENST00000544455.6:c.10076A>C
|
ENSP00000439902.1:p.Glu3359Ala
|
|
ENST00000614259.2:c.10084A>C
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ENSP00000506251.1:n.10084A>C
|
|
ENST00000680887.1:c.10076A>C
|
ENSP00000505508.1:p.Glu3359Ala
|
|
ENST00000380152.7:c.10076A>C
|
ENSP00000369497.3:p.Glu3359Ala
|
|
ENST00000544455.5:c.10076A>C
|
ENSP00000439902.1:p.Glu3359Ala
|
|
NM_000059.3:c.10076A>C , LRG_293t1:c.10076A>C
|
NP_000050.2:p.Glu3359Ala
|
|
XM_011535203.1:c.10076A>C
|
XP_011533505.1:p.Glu3359Ala
|
|
XM_011535204.1:c.9980A>C
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XP_011533506.1:p.Glu3327Ala
|
|
NM_000059.4:c.10076A>C
MANE Select
|
NP_000050.3:p.Glu3359Ala
|
|