ENST00000377833.10:c.10749A=
MANE Select
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ENSP00000367064.4:p.Gly3583=
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ENST00000377833.8:c.10749A=
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ENSP00000367064.4:p.Gly3583=
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NM_001081.3:c.10749A= , LRG_540t1:c.10749A=
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NP_001072.2:p.Gly3583=
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XM_011519709.1:c.6735A=
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XP_011518011.1:p.Gly2245=
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XM_011519710.1:c.6711A=
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XP_011518012.1:p.Gly2237=
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XM_011519711.1:c.6591A=
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XP_011518013.1:p.Gly2197=
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XM_011519709.2:c.6735A=
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XP_011518011.1:p.Gly2245=
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XM_011519710.2:c.6711A=
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XP_011518012.1:p.Gly2237=
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XM_011519711.3:c.6591A=
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XP_011518013.1:p.Gly2197=
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NM_001081.4:c.10749A=
MANE Select
|
NP_001072.2:p.Gly3583=
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