ENST00000399668.7:c.1484A>C
MANE Select
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ENSP00000382576.3:p.Asp495Ala
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ENST00000346991.9:c.1562A>C
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ENSP00000335463.6:p.Asp521Ala
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ENST00000399668.6:c.1484A>C
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ENSP00000382576.2:p.Asp495Ala
|
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ENST00000527044.5:c.1484A>C
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ENSP00000432654.2:p.Asp495Ala
|
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ENST00000533001.1:n.1629A>C
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ENST00000534204.1:c.116-7576A>C
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ENSP00000453857.1:n.116-7576A>C
|
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ENST00000614337.4:n.1800A>C
|
|
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NM_144508.4:c.1484A>C
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NP_653091.3:p.Asp495Ala
|
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NM_170589.4:c.1562A>C
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NP_733468.3:p.Asp521Ala
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XM_011521816.1:c.1160A>C
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XP_011520118.1:p.Asp387Ala
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XM_011521817.1:c.1484A>C
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XP_011520119.1:p.Asp495Ala
|
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XM_017022432.1:c.1160A>C
|
XP_016877921.1:p.Asp387Ala
|
|
NM_144508.5:c.1484A>C
MANE Select
|
NP_653091.3:p.Asp495Ala
|
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NM_170589.5:c.1562A>C
|
NP_733468.3:p.Asp521Ala
|
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