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|
|
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MANE Select
|
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|
|
|
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ENSP00000493749.1:p.Asp1339=
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|
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|
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|
|
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|
|
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|
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|
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|
|
|
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|
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|
|
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|
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|
|
|
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|
ENSP00000495744.1:n.*2305G=
|
|
|
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|
ENSP00000303960.4:p.Asp1341=
|
|
|
ENST00000389817.7:c.4018G=
|
ENSP00000374467.3:p.Asp1340=
|
|
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|
ENSP00000431653.1:n.*1040G=
|
|
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ENST00000528374.1:c.500G=
|
|
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|
|
|
|
ENST00000531891.1:c.357-1G=
|
|
|
|
ENST00000532220.1:n.492G=
|
|
|
|
NM_000352.4:c.4018G=
|
NP_000343.2:p.Asp1340=
|
|
|
NM_001287174.1:c.4021G=
|
NP_001274103.1:p.Asp1341=
|
|
|
XM_011520331.1:c.4018G=
|
XP_011518633.1:p.Asp1340=
|
|
|
XM_011520332.1:c.4021G=
|
XP_011518634.1:p.Asp1341=
|
|
|
XM_011520333.1:c.2518G=
|
XP_011518635.1:p.Asp840=
|
|
|
XR_930890.1:n.4084G=
|
|
|
|
NM_001351295.1:c.4084G=
|
NP_001338224.1:p.Asp1362=
|
|
|
NM_001351296.1:c.4018G=
|
NP_001338225.1:p.Asp1340=
|
|
|
NM_001351297.1:c.4015G=
|
NP_001338226.1:p.Asp1339=
|
|
|
NR_147094.1:n.4313G=
|
|
|
|
XM_017018197.2:c.4087G=
|
XP_016873686.1:p.Asp1363=
|
|
|
XM_017018199.1:c.4084G=
|
XP_016873688.1:p.Asp1362=
|
|
|
XM_017018201.2:c.4087G=
|
XP_016873690.1:p.Asp1363=
|
|
|
XM_017018202.1:c.2584G=
|
XP_016873691.1:p.Asp862=
|
|
|
XM_017018204.1:c.1975G=
|
XP_016873693.1:p.Asp659=
|
|
|
XM_024448668.1:c.2386G=
|
XP_024304436.1:p.Asp796=
|
|
|
XR_001747945.2:n.4159G=
|
|
|
|
XR_001747946.2:n.4090G=
|
|
|
|
XR_002957189.1:n.4755G=
|
|
|
|
NM_000352.6:c.4018G=
MANE Select
|
NP_000343.2:p.Asp1340=
|
|
|
NM_001287174.2:c.4021G=
|
NP_001274103.1:p.Asp1341=
|
|
|
NM_001351295.2:c.4084G=
|
NP_001338224.1:p.Asp1362=
|
|
|
NM_001351296.2:c.4018G=
|
NP_001338225.1:p.Asp1340=
|
|
|
NM_001351297.2:c.4015G=
|
NP_001338226.1:p.Asp1339=
|
|
|
NR_147094.2:n.4313G=
|
|
|
|
NM_001287174.3:c.4021G=
|
NP_001274103.1:p.Asp1341=
|
|
