ENST00000541682.7:c.485C>G
MANE Select
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ENSP00000446205.2:p.Ala162Gly
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ENST00000317814.8:c.470C>G
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ENSP00000314774.4:p.Ala157Gly
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ENST00000541682.6:c.485C>G
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ENSP00000446205.2:p.Ala162Gly
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NM_001165967.1:c.485C>G
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NP_001159439.1:p.Ala162Gly
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NM_032580.3:c.470C>G
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NP_115969.2:p.Ala157Gly
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XM_011524038.1:c.590C>G
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XP_011522340.1:p.Ala197Gly
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XM_011524039.1:c.581C>G
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XP_011522341.1:p.Ala194Gly
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XM_011524040.1:c.581C>G
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XP_011522342.1:p.Ala194Gly
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XM_011524041.1:c.572C>G
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XP_011522343.1:p.Ala191Gly
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XM_011524042.1:c.443C>G
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XP_011522344.1:p.Ala148Gly
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XR_934203.1:n.69+1965G>C
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XM_017025232.1:c.590C>G
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XP_016880721.1:p.Ala197Gly
|
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XM_024451007.1:c.590C>G
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XP_024306775.1:p.Ala197Gly
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NM_001165967.2:c.485C>G
MANE Select
|
NP_001159439.1:p.Ala162Gly
|
|
NM_032580.4:c.470C>G
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NP_115969.2:p.Ala157Gly
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