ENST00000455537.7:c.2937A>T
MANE Select
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ENSP00000408979.2:p.Gly979=
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ENST00000674619.1:c.2958A>T
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ENSP00000502270.1:p.Gly986=
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ENST00000675697.1:c.28A>T
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ENST00000675737.1:n.341A>T
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ENST00000675882.1:n.2460A>T
|
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ENST00000675929.1:n.1495A>T
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ENST00000676055.1:c.28A>T
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ENST00000676457.1:c.2832A>T
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ENSP00000501588.1:p.Gly944=
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ENST00000286452.5:c.2670A>T
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ENSP00000286452.5:p.Gly890=
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ENST00000455537.6:c.2937A>T
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ENSP00000408979.2:p.Gly979=
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ENST00000552227.1:n.220A>T
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NM_004984.2:c.2937A>T
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NP_004975.2:p.Gly979=
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NM_001354705.1:c.2670A>T
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NP_001341634.1:p.Gly890=
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NM_004984.3:c.2937A>T
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NP_004975.2:p.Gly979=
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XR_002957324.1:n.3170A>T
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NM_004984.4:c.2937A>T
MANE Select
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NP_004975.2:p.Gly979=
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NM_001354705.2:c.2670A>T
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NP_001341634.1:p.Gly890=
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