ENST00000274576.9:c.799T>G
MANE Select
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ENSP00000274576.5:p.Trp267Gly
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ENST00000274576.8:c.799T>G
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ENSP00000274576.4:p.Trp267Gly
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ENST00000455880.2:c.799T>G
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ENSP00000411593.2:p.Trp267Gly
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ENST00000462581.6:c.*557T>G
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ENSP00000430595.1:n.*557T>G
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ENST00000471351.2:n.1082T>G
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|
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NM_000171.3:c.799T>G
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NP_000162.2:p.Trp267Gly
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NM_001146040.1:c.799T>G
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NP_001139512.1:p.Trp267Gly
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NM_001292000.1:c.550T>G
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NP_001278929.1:p.Trp184Gly
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XM_005268412.2:c.799T>G
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XP_005268469.1:p.Trp267Gly
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NM_000171.4:c.799T>G
MANE Select
|
NP_000162.2:p.Trp267Gly
|
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NM_001146040.2:c.799T>G
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NP_001139512.1:p.Trp267Gly
|
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NM_001292000.2:c.550T>G
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NP_001278929.1:p.Trp184Gly
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