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ENST00000683365.1:n.4530G=
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ENST00000683693.1:n.5993G=
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ENST00000684157.1:n.5413G=
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|
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|
|
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|
ENSP00000303960.4:p.Asp1406=
|
|
|
ENST00000389817.8:c.4213G=
MANE Select
|
ENSP00000374467.4:p.Asp1405=
|
|
|
ENST00000642271.1:c.4210G=
|
ENSP00000493749.1:p.Asp1404=
|
|
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ENST00000642579.1:c.2267G=
|
|
|
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ENST00000642611.1:n.5431G=
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|
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|
ENST00000642902.1:c.3995G=
|
|
|
|
ENST00000643260.1:c.4213G=
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|
|
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|
|
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|
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|
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|
ENSP00000494567.1:n.*2385G=
|
|
|
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|
ENSP00000495085.1:n.*3202+560G=
|
|
|
ENST00000644772.1:c.4279G=
|
ENSP00000494321.1:p.Asp1427=
|
|
|
ENST00000645004.1:n.1906G=
|
|
|
|
ENST00000645076.1:c.3412G=
|
|
|
|
ENST00000645417.1:c.1401G=
|
|
|
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ENST00000645744.1:c.*3964-66G=
|
ENSP00000494564.1:n.*3964-66G=
|
|
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|
|
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|
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|
ENSP00000495516.1:n.*1496G=
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|
|
ENST00000646003.1:c.*2301-66G=
|
ENSP00000495259.1:n.*2301-66G=
|
|
|
ENST00000646207.1:c.*3050G=
|
ENSP00000495025.1:n.*3050G=
|
|
|
ENST00000646276.1:c.*3617G=
|
ENSP00000496070.1:n.*3617G=
|
|
|
ENST00000646592.1:c.3519G=
|
|
|
|
ENST00000646902.1:c.4180G=
|
ENSP00000494101.1:p.Asp1394=
|
|
|
ENST00000646993.1:c.*2755G=
|
ENSP00000493720.1:n.*2755G=
|
|
|
ENST00000647013.1:c.4219G=
|
ENSP00000496741.1:n.4219G=
|
|
|
ENST00000647015.1:c.3964G=
|
ENSP00000495389.1:p.Asp1322=
|
|
|
ENST00000647086.1:c.*3799G=
|
ENSP00000493677.1:n.*3799G=
|
|
|
ENST00000647158.1:c.*2500G=
|
ENSP00000495744.1:n.*2500G=
|
|
|
ENST00000302539.8:c.4216G=
|
ENSP00000303960.4:p.Asp1406=
|
|
|
ENST00000389817.7:c.4213G=
|
ENSP00000374467.3:p.Asp1405=
|
|
|
ENST00000525022.1:n.212G=
|
|
|
|
ENST00000526037.5:n.77G=
|
|
|
|
ENST00000526168.5:c.67-66G=
|
|
|
|
ENST00000531642.5:c.49G=
|
|
|
|
NM_000352.4:c.4213G=
|
NP_000343.2:p.Asp1405=
|
|
|
NM_001287174.1:c.4216G=
|
NP_001274103.1:p.Asp1406=
|
|
|
XM_011520331.1:c.4213G=
|
XP_011518633.1:p.Asp1405=
|
|
|
XM_011520332.1:c.4216G=
|
XP_011518634.1:p.Asp1406=
|
|
|
XM_011520333.1:c.2713G=
|
XP_011518635.1:p.Asp905=
|
|
|
XR_930890.1:n.4279G=
|
|
|
|
NM_001351295.1:c.4279G=
|
NP_001338224.1:p.Asp1427=
|
|
|
NM_001351296.1:c.4213G=
|
NP_001338225.1:p.Asp1405=
|
|
|
NM_001351297.1:c.4210G=
|
NP_001338226.1:p.Asp1404=
|
|
|
NR_147094.1:n.4508G=
|
|
|
|
XM_017018197.2:c.4282G=
|
XP_016873686.1:p.Asp1428=
|
|
|
XM_017018199.1:c.4279G=
|
XP_016873688.1:p.Asp1427=
|
|
|
XM_017018201.2:c.4282G=
|
XP_016873690.1:p.Asp1428=
|
|
|
XM_017018202.1:c.2779G=
|
XP_016873691.1:p.Asp927=
|
|
|
XM_017018204.1:c.2170G=
|
XP_016873693.1:p.Asp724=
|
|
|
XM_024448668.1:c.2581G=
|
XP_024304436.1:p.Asp861=
|
|
|
XR_001747945.2:n.4354G=
|
|
|
|
XR_001747946.2:n.4285G=
|
|
|
|
XR_002957189.1:n.6068G=
|
|
|
|
NM_000352.6:c.4213G=
MANE Select
|
NP_000343.2:p.Asp1405=
|
|
|
NM_001287174.2:c.4216G=
|
NP_001274103.1:p.Asp1406=
|
|
|
NM_001351295.2:c.4279G=
|
NP_001338224.1:p.Asp1427=
|
|
|
NM_001351296.2:c.4213G=
|
NP_001338225.1:p.Asp1405=
|
|
|
NM_001351297.2:c.4210G=
|
NP_001338226.1:p.Asp1404=
|
|
|
NR_147094.2:n.4508G=
|
|
|
|
NM_001287174.3:c.4216G=
|
NP_001274103.1:p.Asp1406=
|
|
