ENST00000376810.6:c.441T>A
MANE Select
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ENSP00000366006.5:p.Ala147=
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ENST00000376804.2:c.441T>A
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ENSP00000366000.1:p.Ala147=
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ENST00000376810.5:c.441T>A
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ENSP00000366006.5:p.Ala147=
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ENST00000483738.1:c.39T>A
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ENSP00000473453.1:p.Ala13=
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ENST00000486588.6:c.84T>A
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ENSP00000473612.1:p.Ala28=
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NM_013319.2:c.441T>A
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NP_037451.1:p.Ala147=
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XM_006710590.2:c.441T>A
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XP_006710653.1:p.Ala147=
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XM_011541304.1:c.441T>A
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XP_011539606.1:p.Ala147=
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XR_946616.1:n.775T>A
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NM_001330349.1:c.441T>A
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NP_001317278.1:p.Ala147=
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NM_001330350.1:c.441T>A
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NP_001317279.1:p.Ala147=
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XR_946616.3:n.775T>A
|
|
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NM_001330349.2:c.441T>A
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NP_001317278.1:p.Ala147=
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NM_001330350.2:c.441T>A
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NP_001317279.1:p.Ala147=
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NM_013319.3:c.441T>A
MANE Select
|
NP_037451.1:p.Ala147=
|
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