ENST00000527168.6:n.776A>C
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ENST00000529110.2:c.761A>C
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ENSP00000435349.2:p.Glu254Ala
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ENST00000529957.6:n.735A>C
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ENST00000683366.1:c.*409A>C
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ENSP00000507283.1:n.*409A>C
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ENST00000683887.1:c.725A>C
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ENSP00000506886.1:p.Glu242Ala
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ENST00000684100.1:n.671A>C
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ENST00000684126.1:n.811A>C
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ENST00000684688.1:n.1302A>C
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ENST00000204679.9:c.677A>C
MANE Select
|
ENSP00000204679.4:p.Glu226Ala
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ENST00000204679.8:c.677A>C
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ENSP00000204679.4:p.Glu226Ala
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ENST00000527076.1:n.1900A>C
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ENST00000527168.5:n.844A>C
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ENST00000529957.5:n.776A>C
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NM_032520.4:c.677A>C
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NP_115909.1:p.Glu226Ala
|
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XM_017023782.1:c.725A>C
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XP_016879271.1:p.Glu242Ala
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XM_017023783.1:c.317A>C
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XP_016879272.1:p.Glu106Ala
|
|
NM_032520.5:c.677A>C
MANE Select
|
NP_115909.1:p.Glu226Ala
|
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