ENST00000389048.8:c.3551G>T
MANE Select
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ENSP00000373700.3:p.Gly1184Val
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ENST00000431873.6:c.778G>T
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ENST00000638605.1:n.428G>T
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ENST00000642122.1:c.347G>T
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ENSP00000493203.1:p.Gly116Val
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ENST00000389048.7:c.3551G>T
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ENSP00000373700.3:p.Gly1184Val
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ENST00000431873.5:c.431G>T
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ENSP00000414027.2:p.Gly144Val
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ENST00000618119.4:c.2420G>T
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ENSP00000482733.1:p.Gly807Val
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NM_004304.4:c.3551G>T
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NP_004295.2:p.Gly1184Val
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NM_001353765.1:c.347G>T
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NP_001340694.1:p.Gly116Val
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XM_024452778.1:c.704G>T
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XP_024308546.1:p.Gly235Val
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XM_024452779.1:c.347G>T
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XP_024308547.1:p.Gly116Val
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NM_004304.5:c.3551G>T
MANE Select
|
NP_004295.2:p.Gly1184Val
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NM_001353765.2:c.347G>T
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NP_001340694.1:p.Gly116Val
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