ENST00000357578.8:c.595G=
MANE Select
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ENSP00000350191.3:p.Ala199=
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ENST00000672352.1:c.358G=
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ENSP00000500876.1:p.Ala120=
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ENST00000672557.1:c.513G=
|
|
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ENST00000672652.1:c.516G=
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|
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ENST00000675422.1:n.1355G=
|
|
|
ENST00000348925.2:c.595G=
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ENSP00000314649.3:p.Ala199=
|
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ENST00000357578.7:c.595G=
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ENSP00000350191.3:p.Ala199=
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ENST00000491546.5:c.511G=
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ENSP00000417687.1:p.Ala171=
|
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NM_001080.3:c.595G=
MANE Select
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NP_001071.1:p.Ala199=
|
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NM_170740.1:c.595G=
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NP_733936.1:p.Ala199=
|
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NM_001368954.1:c.595G=
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NP_001355883.1:p.Ala199=
|
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