ENST00000474887.6:c.563T>A
|
|
|
ENST00000683393.1:c.1390T>A
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ENSP00000508654.1:n.1390T>A
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ENST00000683760.1:c.1575T>A
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ENSP00000507765.1:p.Asp525Glu
|
|
ENST00000321117.10:c.2244T>A
MANE Select
|
ENSP00000324375.5:p.Asp748Glu
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|
ENST00000264709.7:c.2244T>A
|
ENSP00000264709.3:p.Asp748Glu
|
|
ENST00000321117.9:c.2244T>A
|
ENSP00000324375.5:p.Asp748Glu
|
|
ENST00000380746.8:c.1677T>A
|
ENSP00000370122.4:p.Asp559Glu
|
|
ENST00000380756.7:c.2244T>A
|
ENSP00000370132.3:p.Asp748Glu
|
|
ENST00000402667.1:c.1575T>A
|
ENSP00000384237.1:p.Asp525Glu
|
|
ENST00000461228.1:n.463T>A
|
|
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ENST00000466601.5:n.616T>A
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|
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ENST00000474887.5:n.563T>A
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|
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ENST00000482935.5:n.244T>A
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|
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ENST00000491288.5:n.310+260T>A
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|
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NM_022552.4:c.2244T>A , LRG_459t1:c.2244T>A
|
NP_072046.2:p.Asp748Glu
|
|
NM_153759.3:c.1677T>A , LRG_459t2:c.1677T>A
|
NP_715640.2:p.Asp559Glu
|
|
NM_175629.2:c.2244T>A , LRG_459t4:c.2244T>A
|
NP_783328.1:p.Asp748Glu
|
|
XM_005264175.3:c.2244T>A
|
XP_005264232.1:p.Asp748Glu
|
|
XM_005264177.3:c.1575T>A
|
XP_005264234.1:p.Asp525Glu
|
|
XM_006711957.2:c.2244T>A
|
XP_006712020.1:p.Asp748Glu
|
|
XM_006711958.2:c.1800T>A
|
XP_006712021.1:p.Asp600Glu
|
|
XM_011532662.1:c.2097T>A
|
XP_011530964.1:p.Asp699Glu
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|
XM_011532663.1:c.2079T>A
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XP_011530965.1:p.Asp693Glu
|
|
XM_011532664.1:c.2244T>A
|
XP_011530966.1:p.Asp748Glu
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|
XM_011532665.1:c.1788T>A
|
XP_011530967.1:p.Asp596Glu
|
|
XM_011532666.1:c.1716T>A
|
XP_011530968.1:p.Asp572Glu
|
|
XM_011532667.1:c.1575T>A
|
XP_011530969.1:p.Asp525Glu
|
|
XM_011532668.1:c.2244T>A
|
XP_011530970.1:p.Asp748Glu
|
|
NM_001320893.1:c.1788T>A
|
NP_001307822.1:p.Asp596Glu
|
|
NR_135490.1:n.2582T>A
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|
|
XM_005264175.5:c.2244T>A
|
XP_005264232.1:p.Asp748Glu
|
|
XM_005264177.4:c.1575T>A
|
XP_005264234.1:p.Asp525Glu
|
|
XM_011532662.2:c.2097T>A
|
XP_011530964.1:p.Asp699Glu
|
|
XM_011532663.2:c.2079T>A
|
XP_011530965.1:p.Asp693Glu
|
|
XM_011532664.2:c.2244T>A
|
XP_011530966.1:p.Asp748Glu
|
|
XM_011532666.2:c.1716T>A
|
XP_011530968.1:p.Asp572Glu
|
|
XM_011532667.3:c.1575T>A
|
XP_011530969.1:p.Asp525Glu
|
|
XM_017003526.1:c.2244T>A
|
XP_016859015.1:p.Asp748Glu
|
|
XM_017003527.1:c.1575T>A
|
XP_016859016.1:p.Asp525Glu
|
|
XR_001738657.1:n.2521T>A
|
|
|
NM_001375819.1:c.1575T>A
|
NP_001362748.1:p.Asp525Glu
|
|
NR_135490.2:n.2475T>A
|
|
|
NM_022552.5:c.2244T>A
MANE Select
|
NP_072046.2:p.Asp748Glu
|
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