ENST00000527168.6:n.881G>C
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ENST00000529110.2:c.866G>C
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ENSP00000435349.2:p.Gly289Ala
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ENST00000529957.6:n.840G>C
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ENST00000683366.1:c.*514G>C
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ENSP00000507283.1:n.*514G>C
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ENST00000683887.1:c.830G>C
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ENSP00000506886.1:p.Gly277Ala
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ENST00000684100.1:n.776G>C
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ENST00000684126.1:n.916G>C
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ENST00000684688.1:n.1407G>C
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ENST00000204679.9:c.782G>C
MANE Select
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ENSP00000204679.4:p.Gly261Ala
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ENST00000204679.8:c.782G>C
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ENSP00000204679.4:p.Gly261Ala
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ENST00000527076.1:n.2005G>C
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ENST00000527168.5:n.949G>C
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ENST00000529957.5:n.881G>C
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NM_032520.4:c.782G>C
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NP_115909.1:p.Gly261Ala
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XM_017023782.1:c.830G>C
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XP_016879271.1:p.Gly277Ala
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XM_017023783.1:c.422G>C
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XP_016879272.1:p.Gly141Ala
|
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NM_032520.5:c.782G>C
MANE Select
|
NP_115909.1:p.Gly261Ala
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