ENST00000541682.7:c.242G>T
MANE Select
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ENSP00000446205.2:p.Gly81Val
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ENST00000317814.8:c.227G>T
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ENSP00000314774.4:p.Gly76Val
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ENST00000541682.6:c.242G>T
|
ENSP00000446205.2:p.Gly81Val
|
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ENST00000577735.1:c.218G>T
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ENSP00000462491.1:p.Gly73Val
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NM_001165967.1:c.242G>T
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NP_001159439.1:p.Gly81Val
|
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NM_032580.3:c.227G>T
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NP_115969.2:p.Gly76Val
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XM_011524038.1:c.347G>T
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XP_011522340.1:p.Gly116Val
|
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XM_011524039.1:c.338G>T
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XP_011522341.1:p.Gly113Val
|
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XM_011524040.1:c.338G>T
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XP_011522342.1:p.Gly113Val
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XM_011524041.1:c.329G>T
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XP_011522343.1:p.Gly110Val
|
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XM_011524042.1:c.200G>T
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XP_011522344.1:p.Gly67Val
|
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XR_934203.1:n.69+2208C>A
|
|
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XM_017025232.1:c.347G>T
|
XP_016880721.1:p.Gly116Val
|
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XM_024451007.1:c.347G>T
|
XP_024306775.1:p.Gly116Val
|
|
NM_001165967.2:c.242G>T
MANE Select
|
NP_001159439.1:p.Gly81Val
|
|
NM_032580.4:c.227G>T
|
NP_115969.2:p.Gly76Val
|
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