ENST00000274576.9:c.1181_1182delinsCT
MANE Select
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ENSP00000274576.5:p.Pro394=
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ENST00000274576.8:c.1181_1182delinsCT
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ENSP00000274576.4:p.Pro394=
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ENST00000455880.2:c.1205_1206delinsCT
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ENSP00000411593.2:p.Pro402=
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ENST00000462581.6:c.*939_*940delinsCT
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ENSP00000430595.1:n.*939_*940delinsCT
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NM_000171.3:c.1181_1182delinsCT
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NP_000162.2:p.Pro394=
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|
NM_001146040.1:c.1205_1206delinsCT
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NP_001139512.1:p.Pro402=
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NM_001292000.1:c.932_933delinsCT
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NP_001278929.1:p.Pro311=
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|
NM_000171.4:c.1181_1182delinsCT
MANE Select
|
NP_000162.2:p.Pro394=
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|
NM_001146040.2:c.1205_1206delinsCT
|
NP_001139512.1:p.Pro402=
|
|
NM_001292000.2:c.932_933delinsCT
|
NP_001278929.1:p.Pro311=
|
|