ENST00000352480.10:c.860G>T
MANE Select
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ENSP00000253004.6:p.Gly287Val
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ENST00000352480.9:c.860G>T
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ENSP00000253004.6:p.Gly287Val
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ENST00000372386.6:n.131G>T
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ENST00000372393.7:c.860G>T
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ENSP00000361469.2:p.Gly287Val
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ENST00000372394.5:c.860G>T
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ENSP00000361471.1:p.Gly287Val
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ENST00000470849.4:n.585G>T
|
|
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ENST00000492400.5:n.369G>T
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ENST00000493984.6:n.637G>T
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NM_000050.4:c.860G>T
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NP_000041.2:p.Gly287Val
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NM_054012.3:c.860G>T
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NP_446464.1:p.Gly287Val
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XM_005272200.2:c.860G>T
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XP_005272257.1:p.Gly287Val
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XM_011518705.1:c.974G>T
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XP_011517007.1:p.Gly325Val
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XM_005272200.3:c.860G>T
|
XP_005272257.1:p.Gly287Val
|
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XM_011518705.2:c.974G>T
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XP_011517007.1:p.Gly325Val
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XM_017014729.1:c.956G>T
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XP_016870218.1:p.Gly319Val
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NM_054012.4:c.860G>T
MANE Select
|
NP_446464.1:p.Gly287Val
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