ENST00000541682.7:c.356C>G
MANE Select
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ENSP00000446205.2:p.Ala119Gly
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ENST00000317814.8:c.341C>G
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ENSP00000314774.4:p.Ala114Gly
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ENST00000541682.6:c.356C>G
|
ENSP00000446205.2:p.Ala119Gly
|
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ENST00000577735.1:c.332C>G
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ENSP00000462491.1:p.Ala111Gly
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NM_001165967.1:c.356C>G
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NP_001159439.1:p.Ala119Gly
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NM_032580.3:c.341C>G
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NP_115969.2:p.Ala114Gly
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XM_011524038.1:c.461C>G
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XP_011522340.1:p.Ala154Gly
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XM_011524039.1:c.452C>G
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XP_011522341.1:p.Ala151Gly
|
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XM_011524040.1:c.452C>G
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XP_011522342.1:p.Ala151Gly
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XM_011524041.1:c.443C>G
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XP_011522343.1:p.Ala148Gly
|
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XM_011524042.1:c.314C>G
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XP_011522344.1:p.Ala105Gly
|
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XR_934203.1:n.69+2094G>C
|
|
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XM_017025232.1:c.461C>G
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XP_016880721.1:p.Ala154Gly
|
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XM_024451007.1:c.461C>G
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XP_024306775.1:p.Ala154Gly
|
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NM_001165967.2:c.356C>G
MANE Select
|
NP_001159439.1:p.Ala119Gly
|
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NM_032580.4:c.341C>G
|
NP_115969.2:p.Ala114Gly
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