ENST00000315491.12:c.1214A>C
MANE Select
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ENSP00000320295.7:p.Glu405Ala
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ENST00000680788.1:n.4635A>C
|
|
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ENST00000315491.11:c.1214A>C
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ENSP00000320295.7:p.Glu405Ala
|
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ENST00000554444.5:c.998A>C
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ENSP00000451617.1:p.Glu333Ala
|
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ENST00000555576.5:c.277+2087A>C
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ENSP00000452554.1:n.277+2087A>C
|
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ENST00000555609.5:c.*1299A>C
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ENSP00000451276.1:n.*1299A>C
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ENST00000556922.1:c.2255A>C
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ENSP00000451560.1:p.Glu752Ala
|
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NM_001197181.1:c.998A>C
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NP_001184110.1:p.Glu333Ala
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NM_006086.3:c.1214A>C
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NP_006077.2:p.Glu405Ala
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NM_006086.4:c.1214A>C
MANE Select
|
NP_006077.2:p.Glu405Ala
|
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NM_001197181.2:c.998A>C
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NP_001184110.1:p.Glu333Ala
|
|