ENST00000541682.7:c.638G>T
MANE Select
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ENSP00000446205.2:p.Gly213Val
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ENST00000317814.8:c.623G>T
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ENSP00000314774.4:p.Gly208Val
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|
ENST00000541682.6:c.638G>T
|
ENSP00000446205.2:p.Gly213Val
|
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NM_001165967.1:c.638G>T
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NP_001159439.1:p.Gly213Val
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NM_032580.3:c.623G>T
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NP_115969.2:p.Gly208Val
|
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XM_011524038.1:c.743G>T
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XP_011522340.1:p.Gly248Val
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XM_011524039.1:c.734G>T
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XP_011522341.1:p.Gly245Val
|
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XM_011524040.1:c.734G>T
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XP_011522342.1:p.Gly245Val
|
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XM_011524041.1:c.725G>T
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XP_011522343.1:p.Gly242Val
|
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XM_011524042.1:c.596G>T
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XP_011522344.1:p.Gly199Val
|
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XR_934203.1:n.69+1812C>A
|
|
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XM_017025232.1:c.743G>T
|
XP_016880721.1:p.Gly248Val
|
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XM_024451007.1:c.743G>T
|
XP_024306775.1:p.Gly248Val
|
|
NM_001165967.2:c.638G>T
MANE Select
|
NP_001159439.1:p.Gly213Val
|
|
NM_032580.4:c.623G>T
|
NP_115969.2:p.Gly208Val
|
|