ENST00000541682.7:c.281C>G
MANE Select
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ENSP00000446205.2:p.Ala94Gly
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ENST00000317814.8:c.266C>G
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ENSP00000314774.4:p.Ala89Gly
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ENST00000541682.6:c.281C>G
|
ENSP00000446205.2:p.Ala94Gly
|
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ENST00000577735.1:c.257C>G
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ENSP00000462491.1:p.Ala86Gly
|
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NM_001165967.1:c.281C>G
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NP_001159439.1:p.Ala94Gly
|
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NM_032580.3:c.266C>G
|
NP_115969.2:p.Ala89Gly
|
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XM_011524038.1:c.386C>G
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XP_011522340.1:p.Ala129Gly
|
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XM_011524039.1:c.377C>G
|
XP_011522341.1:p.Ala126Gly
|
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XM_011524040.1:c.377C>G
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XP_011522342.1:p.Ala126Gly
|
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XM_011524041.1:c.368C>G
|
XP_011522343.1:p.Ala123Gly
|
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XM_011524042.1:c.239C>G
|
XP_011522344.1:p.Ala80Gly
|
|
XR_934203.1:n.69+2169G>C
|
|
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XM_017025232.1:c.386C>G
|
XP_016880721.1:p.Ala129Gly
|
|
XM_024451007.1:c.386C>G
|
XP_024306775.1:p.Ala129Gly
|
|
NM_001165967.2:c.281C>G
MANE Select
|
NP_001159439.1:p.Ala94Gly
|
|
NM_032580.4:c.266C>G
|
NP_115969.2:p.Ala89Gly
|
|