ENST00000242317.9:c.1820C>G
MANE Select
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ENSP00000242317.4:p.Ala607Gly
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ENST00000242317.8:c.1820C>G
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ENSP00000242317.4:p.Ala607Gly
|
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ENST00000442556.1:c.329+2547C>G
|
|
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ENST00000470169.5:c.608C>G
|
|
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ENST00000485580.1:n.396C>G
|
|
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ENST00000614641.4:c.1832C>G
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ENSP00000480538.1:p.Ala611Gly
|
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NM_001281428.1:c.1832C>G
|
NP_001268357.1:p.Ala611Gly
|
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NM_012144.3:c.1820C>G
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NP_036276.1:p.Ala607Gly
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XM_006716758.2:c.1289C>G
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XP_006716821.1:p.Ala430Gly
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XM_011517848.1:c.1574C>G
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XP_011516150.1:p.Ala525Gly
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XM_006716758.3:c.1289C>G
|
XP_006716821.1:p.Ala430Gly
|
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XM_011517848.2:c.1574C>G
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XP_011516150.1:p.Ala525Gly
|
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XM_017014625.2:c.1562C>G
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XP_016870114.1:p.Ala521Gly
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XR_002956774.1:n.1923C>G
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NM_012144.4:c.1820C>G
MANE Select
|
NP_036276.1:p.Ala607Gly
|
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NM_001281428.2:c.1832C>G
|
NP_001268357.1:p.Ala611Gly
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