ENST00000290866.10:c.2493A=
MANE Select
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ENSP00000290866.4:p.Thr831=
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ENST00000290863.10:c.771A=
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ENSP00000290863.6:p.Thr257=
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ENST00000290866.9:c.2493A=
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ENSP00000290866.4:p.Thr831=
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ENST00000413513.7:c.771A=
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ENSP00000392247.3:p.Thr257=
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ENST00000428043.5:c.2493A=
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ENSP00000397593.2:p.Thr831=
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|
ENST00000577647.2:c.771A=
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ENSP00000464149.1:p.Thr257=
|
|
ENST00000578839.5:c.*519+193A=
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ENSP00000462110.2:n.*519+193A=
|
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ENST00000579204.1:c.752A=
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ENSP00000464629.1:n.752A=
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ENST00000579314.5:c.*222A=
|
ENSP00000462599.1:n.*222A=
|
|
ENST00000582005.5:c.*413A=
|
ENSP00000462002.1:n.*413A=
|
|
ENST00000582761.1:c.261A=
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ENSP00000462909.1:p.Thr87=
|
|
ENST00000584865.5:n.439A=
|
|
|
NM_000789.3:c.2493A=
|
NP_000780.1:p.Thr831=
|
|
NM_001178057.1:c.771A=
|
NP_001171528.1:p.Thr257=
|
|
NM_152830.2:c.771A=
|
NP_690043.1:p.Thr257=
|
|
XM_005257110.1:c.1944A=
|
XP_005257167.1:p.Thr648=
|
|
XM_006721737.2:c.831A=
|
XP_006721800.2:p.Thr277=
|
|
XM_006721737.3:c.831A=
|
XP_006721800.2:p.Thr277=
|
|
NM_000789.4:c.2493A=
MANE Select
|
NP_000780.1:p.Thr831=
|
|
NM_001178057.2:c.771A=
|
NP_001171528.1:p.Thr257=
|
|
NM_152830.3:c.771A=
|
NP_690043.1:p.Thr257=
|
|
NM_001382700.1:c.1926A=
|
NP_001369629.1:p.Thr642=
|
|
NM_001382701.1:c.1641A=
|
NP_001369630.1:p.Thr547=
|
|
NM_001382702.1:c.379+193A=
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NP_001369631.1:n.379+193A=
|
|
NR_168483.1:n.871A=
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|
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