ENST00000557088.6:c.*1005A>G
|
ENSP00000451002.1:n.*1005A>G
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ENST00000557570.2:c.871A>G
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ENSP00000450787.2:p.Thr291Ala
|
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ENST00000706675.1:n.854A>G
|
|
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ENST00000706676.1:c.1213A>G
|
ENSP00000516492.1:p.Thr405Ala
|
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ENST00000706677.1:c.1039A>G
|
ENSP00000516493.1:p.Thr347Ala
|
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ENST00000706678.1:n.959A>G
|
|
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ENST00000706679.1:c.871A>G
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ENSP00000516494.1:p.Thr291Ala
|
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ENST00000706680.1:c.*882A>G
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ENSP00000516495.1:n.*882A>G
|
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ENST00000706681.1:c.*778A>G
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ENSP00000516496.1:n.*778A>G
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ENST00000342058.9:c.1039A>G
MANE Select
|
ENSP00000345008.4:p.Thr347Ala
|
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ENST00000267620.14:c.1162A>G
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ENSP00000267620.10:p.Thr388Ala
|
|
ENST00000342058.8:c.1039A>G
|
ENSP00000345008.4:p.Thr347Ala
|
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ENST00000554121.2:n.165A>G
|
|
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ENST00000556154.5:c.1054A>G
|
ENSP00000451982.1:p.Thr352Ala
|
|
NM_006329.3:c.1039A>G , LRG_364t1:c.1039A>G
|
NP_006320.2:p.Thr347Ala
|
|
XM_005267267.3:c.1090A>G
|
XP_005267324.1:p.Thr364Ala
|
|
XM_011536356.1:c.1090A>G
|
XP_011534658.1:p.Thr364Ala
|
|
XM_011536357.1:c.1039A>G
|
XP_011534659.1:p.Thr347Ala
|
|
XM_011536358.1:c.871A>G
|
XP_011534660.1:p.Thr291Ala
|
|
XM_011536357.2:c.1039A>G
|
XP_011534659.1:p.Thr347Ala
|
|
XM_011536358.2:c.871A>G
|
XP_011534660.1:p.Thr291Ala
|
|
XM_017020929.2:c.871A>G
|
XP_016876418.1:p.Thr291Ala
|
|
NM_001384158.1:c.1162A>G
|
NP_001371087.1:p.Thr388Ala
|
|
NM_001384159.1:c.1090A>G
|
NP_001371088.1:p.Thr364Ala
|
|
NM_001384160.1:c.1039A>G
|
NP_001371089.1:p.Thr347Ala
|
|
NM_001384161.1:c.871A>G
|
NP_001371090.1:p.Thr291Ala
|
|
NM_001384162.1:c.871A>G
|
NP_001371091.1:p.Thr291Ala
|
|
NM_006329.4:c.1039A>G
MANE Select
|
NP_006320.2:p.Thr347Ala
|
|