ENST00000389048.8:c.3797C>A
MANE Select
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ENSP00000373700.3:p.Ala1266Asp
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ENST00000431873.6:c.1024C>A
|
|
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ENST00000638605.1:n.674C>A
|
|
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ENST00000642122.1:c.593C>A
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ENSP00000493203.1:p.Ala198Asp
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ENST00000389048.7:c.3797C>A
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ENSP00000373700.3:p.Ala1266Asp
|
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ENST00000431873.5:c.677C>A
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ENSP00000414027.2:p.Ala226Asp
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ENST00000618119.4:c.2666C>A
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ENSP00000482733.1:p.Ala889Asp
|
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NM_004304.4:c.3797C>A
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NP_004295.2:p.Ala1266Asp
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NM_001353765.1:c.593C>A
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NP_001340694.1:p.Ala198Asp
|
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XM_024452778.1:c.950C>A
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XP_024308546.1:p.Ala317Asp
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XM_024452779.1:c.593C>A
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XP_024308547.1:p.Ala198Asp
|
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NM_004304.5:c.3797C>A
MANE Select
|
NP_004295.2:p.Ala1266Asp
|
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NM_001353765.2:c.593C>A
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NP_001340694.1:p.Ala198Asp
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