ENST00000242317.9:c.1881C>G
MANE Select
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ENSP00000242317.4:p.Ala627=
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ENST00000242317.8:c.1881C>G
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ENSP00000242317.4:p.Ala627=
|
|
ENST00000442556.1:c.329+2608C>G
|
|
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ENST00000470169.5:c.669C>G
|
|
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ENST00000485580.1:n.457C>G
|
|
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ENST00000614641.4:c.1893C>G
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ENSP00000480538.1:p.Ala631=
|
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NM_001281428.1:c.1893C>G
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NP_001268357.1:p.Ala631=
|
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NM_012144.3:c.1881C>G
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NP_036276.1:p.Ala627=
|
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XM_006716758.2:c.1350C>G
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XP_006716821.1:p.Ala450=
|
|
XM_011517848.1:c.1635C>G
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XP_011516150.1:p.Ala545=
|
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XM_006716758.3:c.1350C>G
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XP_006716821.1:p.Ala450=
|
|
XM_011517848.2:c.1635C>G
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XP_011516150.1:p.Ala545=
|
|
XM_017014625.2:c.1623C>G
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XP_016870114.1:p.Ala541=
|
|
XR_002956774.1:n.1984C>G
|
|
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NM_012144.4:c.1881C>G
MANE Select
|
NP_036276.1:p.Ala627=
|
|
NM_001281428.2:c.1893C>G
|
NP_001268357.1:p.Ala631=
|
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