ENST00000352511.5:c.1214G>C
MANE Select
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ENSP00000340361.3:p.Gly405Ala
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ENST00000352511.4:c.1214G>C
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ENSP00000340361.3:p.Gly405Ala
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ENST00000461232.1:n.5003G>C
|
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ENST00000465020.5:n.1300G>C
|
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NM_001106.3:c.1214G>C
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NP_001097.2:p.Gly405Ala
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XM_005265583.2:c.1277G>C
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XP_005265640.1:p.Gly426Ala
|
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XM_005265583.3:c.1277G>C
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XP_005265640.1:p.Gly426Ala
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XM_017007514.1:c.1256G>C
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XP_016863003.1:p.Gly419Ala
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XM_017007515.2:c.1232G>C
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XP_016863004.1:p.Gly411Ala
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XM_017007516.1:c.1211G>C
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XP_016863005.1:p.Gly404Ala
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NM_001106.4:c.1214G>C
MANE Select
|
NP_001097.2:p.Gly405Ala
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