ENST00000290866.10:c.3681G=
MANE Select
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ENSP00000290866.4:p.Thr1227=
|
|
ENST00000290863.10:c.1959G=
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ENSP00000290863.6:p.Thr653=
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ENST00000290866.9:c.3681G=
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ENSP00000290866.4:p.Thr1227=
|
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ENST00000413513.7:c.1836G=
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ENSP00000392247.3:p.Thr612=
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|
ENST00000428043.5:c.3681G=
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ENSP00000397593.2:p.Thr1227=
|
|
ENST00000577418.5:n.691G=
|
|
|
ENST00000577647.2:c.1959G=
|
ENSP00000464149.1:p.Thr653=
|
|
ENST00000578839.5:c.*1436G=
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ENSP00000462110.2:n.*1436G=
|
|
ENST00000579314.5:c.*1410G=
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ENSP00000462599.1:n.*1410G=
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|
ENST00000579409.1:c.368G=
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|
|
ENST00000582244.1:n.555G=
|
|
|
NM_000789.3:c.3681G=
|
NP_000780.1:p.Thr1227=
|
|
NM_001178057.1:c.1836G=
|
NP_001171528.1:p.Thr612=
|
|
NM_152830.2:c.1959G=
|
NP_690043.1:p.Thr653=
|
|
XM_005257110.1:c.3132G=
|
XP_005257167.1:p.Thr1044=
|
|
XM_006721737.2:c.2019G=
|
XP_006721800.2:p.Thr673=
|
|
XM_006721737.3:c.2019G=
|
XP_006721800.2:p.Thr673=
|
|
NM_000789.4:c.3681G=
MANE Select
|
NP_000780.1:p.Thr1227=
|
|
NM_001178057.2:c.1836G=
|
NP_001171528.1:p.Thr612=
|
|
NM_152830.3:c.1959G=
|
NP_690043.1:p.Thr653=
|
|
NM_001382700.1:c.3114G=
|
NP_001369629.1:p.Thr1038=
|
|
NM_001382701.1:c.2829G=
|
NP_001369630.1:p.Thr943=
|
|
NM_001382702.1:c.1296G=
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NP_001369631.1:p.Thr432=
|
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NR_168483.1:n.2059G=
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|
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