ENST00000290866.10:c.2367C>T
MANE Select
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ENSP00000290866.4:p.Gly789=
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ENST00000290863.10:c.645C>T
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ENSP00000290863.6:p.Gly215=
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ENST00000290866.9:c.2367C>T
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ENSP00000290866.4:p.Gly789=
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ENST00000413513.7:c.645C>T
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ENSP00000392247.3:p.Gly215=
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ENST00000428043.5:c.2367C>T
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ENSP00000397593.2:p.Gly789=
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ENST00000577647.2:c.645C>T
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ENSP00000464149.1:p.Gly215=
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ENST00000578839.5:c.*437C>T
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ENSP00000462110.2:n.*437C>T
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ENST00000579204.1:c.626C>T
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ENSP00000464629.1:n.626C>T
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ENST00000579314.5:c.*96C>T
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ENSP00000462599.1:n.*96C>T
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ENST00000582005.5:c.*287C>T
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ENSP00000462002.1:n.*287C>T
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ENST00000582761.1:c.135C>T
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ENSP00000462909.1:p.Gly45=
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ENST00000584865.5:n.313C>T
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|
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NM_000789.3:c.2367C>T
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NP_000780.1:p.Gly789=
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NM_001178057.1:c.645C>T
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NP_001171528.1:p.Gly215=
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NM_152830.2:c.645C>T
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NP_690043.1:p.Gly215=
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XM_005257110.1:c.1818C>T
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XP_005257167.1:p.Gly606=
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XM_006721737.2:c.705C>T
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XP_006721800.2:p.Gly235=
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XM_006721737.3:c.705C>T
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XP_006721800.2:p.Gly235=
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NM_000789.4:c.2367C>T
MANE Select
|
NP_000780.1:p.Gly789=
|
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NM_001178057.2:c.645C>T
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NP_001171528.1:p.Gly215=
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NM_152830.3:c.645C>T
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NP_690043.1:p.Gly215=
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NM_001382700.1:c.1800C>T
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NP_001369629.1:p.Gly600=
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NM_001382701.1:c.1515C>T
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NP_001369630.1:p.Gly505=
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NM_001382702.1:c.297C>T
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NP_001369631.1:p.Gly99=
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NR_168483.1:n.745C>T
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