ENST00000541682.7:c.353C>G
MANE Select
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ENSP00000446205.2:p.Ala118Gly
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ENST00000317814.8:c.338C>G
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ENSP00000314774.4:p.Ala113Gly
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ENST00000541682.6:c.353C>G
|
ENSP00000446205.2:p.Ala118Gly
|
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ENST00000577735.1:c.329C>G
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ENSP00000462491.1:p.Ala110Gly
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NM_001165967.1:c.353C>G
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NP_001159439.1:p.Ala118Gly
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NM_032580.3:c.338C>G
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NP_115969.2:p.Ala113Gly
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XM_011524038.1:c.458C>G
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XP_011522340.1:p.Ala153Gly
|
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XM_011524039.1:c.449C>G
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XP_011522341.1:p.Ala150Gly
|
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XM_011524040.1:c.449C>G
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XP_011522342.1:p.Ala150Gly
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XM_011524041.1:c.440C>G
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XP_011522343.1:p.Ala147Gly
|
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XM_011524042.1:c.311C>G
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XP_011522344.1:p.Ala104Gly
|
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XR_934203.1:n.69+2097G>C
|
|
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XM_017025232.1:c.458C>G
|
XP_016880721.1:p.Ala153Gly
|
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XM_024451007.1:c.458C>G
|
XP_024306775.1:p.Ala153Gly
|
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NM_001165967.2:c.353C>G
MANE Select
|
NP_001159439.1:p.Ala118Gly
|
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NM_032580.4:c.338C>G
|
NP_115969.2:p.Ala113Gly
|
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