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|
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|
ENSP00000303960.4:p.Asp1355=
|
|
|
ENST00000389817.8:c.4060G=
MANE Select
|
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|
|
|
ENST00000642271.1:c.4057G=
|
ENSP00000493749.1:p.Asp1353=
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|
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|
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|
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ENST00000643260.1:c.4060G=
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|
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|
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|
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|
ENSP00000495085.1:n.*2491G=
|
|
|
ENST00000644772.1:c.4126G=
|
ENSP00000494321.1:p.Asp1376=
|
|
|
ENST00000645004.1:n.1715G=
|
|
|
|
ENST00000645076.1:c.3259G=
|
|
|
|
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|
|
|
|
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|
ENSP00000494564.1:n.*2840G=
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|
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|
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ENSP00000495259.1:n.*2162G=
|
|
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|
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ENSP00000496070.1:n.*2479G=
|
|
|
ENST00000646592.1:c.3366G=
|
|
|
|
ENST00000646902.1:c.4027G=
|
ENSP00000494101.1:p.Asp1343=
|
|
|
ENST00000646993.1:c.*2602G=
|
ENSP00000493720.1:n.*2602G=
|
|
|
ENST00000647013.1:c.4066G=
|
ENSP00000496741.1:n.4066G=
|
|
|
ENST00000647015.1:c.3811G=
|
ENSP00000495389.1:p.Asp1271=
|
|
|
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|
ENSP00000493677.1:n.*3646G=
|
|
|
ENST00000647158.1:c.*2347G=
|
ENSP00000495744.1:n.*2347G=
|
|
|
ENST00000302539.8:c.4063G=
|
ENSP00000303960.4:p.Asp1355=
|
|
|
ENST00000389817.7:c.4060G=
|
ENSP00000374467.3:p.Asp1354=
|
|
|
ENST00000527905.5:c.*1082G=
|
ENSP00000431653.1:n.*1082G=
|
|
|
ENST00000528374.1:c.542G=
|
|
|
|
ENST00000531137.1:n.625G=
|
|
|
|
ENST00000531891.1:c.398G=
|
|
|
|
ENST00000532220.1:n.534G=
|
|
|
|
NM_000352.4:c.4060G=
|
NP_000343.2:p.Asp1354=
|
|
|
NM_001287174.1:c.4063G=
|
NP_001274103.1:p.Asp1355=
|
|
|
XM_011520331.1:c.4060G=
|
XP_011518633.1:p.Asp1354=
|
|
|
XM_011520332.1:c.4063G=
|
XP_011518634.1:p.Asp1355=
|
|
|
XM_011520333.1:c.2560G=
|
XP_011518635.1:p.Asp854=
|
|
|
XR_930890.1:n.4126G=
|
|
|
|
NM_001351295.1:c.4126G=
|
NP_001338224.1:p.Asp1376=
|
|
|
NM_001351296.1:c.4060G=
|
NP_001338225.1:p.Asp1354=
|
|
|
NM_001351297.1:c.4057G=
|
NP_001338226.1:p.Asp1353=
|
|
|
NR_147094.1:n.4355G=
|
|
|
|
XM_017018197.2:c.4129G=
|
XP_016873686.1:p.Asp1377=
|
|
|
XM_017018199.1:c.4126G=
|
XP_016873688.1:p.Asp1376=
|
|
|
XM_017018201.2:c.4129G=
|
XP_016873690.1:p.Asp1377=
|
|
|
XM_017018202.1:c.2626G=
|
XP_016873691.1:p.Asp876=
|
|
|
XM_017018204.1:c.2017G=
|
XP_016873693.1:p.Asp673=
|
|
|
XM_024448668.1:c.2428G=
|
XP_024304436.1:p.Asp810=
|
|
|
XR_001747945.2:n.4201G=
|
|
|
|
XR_001747946.2:n.4132G=
|
|
|
|
XR_002957189.1:n.4797G=
|
|
|
|
NM_000352.6:c.4060G=
MANE Select
|
NP_000343.2:p.Asp1354=
|
|
|
NM_001287174.2:c.4063G=
|
NP_001274103.1:p.Asp1355=
|
|
|
NM_001351295.2:c.4126G=
|
NP_001338224.1:p.Asp1376=
|
|
|
NM_001351296.2:c.4060G=
|
NP_001338225.1:p.Asp1354=
|
|
|
NM_001351297.2:c.4057G=
|
NP_001338226.1:p.Asp1353=
|
|
|
NR_147094.2:n.4355G=
|
|
|
|
NM_001287174.3:c.4063G=
|
NP_001274103.1:p.Asp1355=
|
|
