ENST00000218099.7:c.350G>T
MANE Select
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ENSP00000218099.2:p.Cys117Phe
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ENST00000218099.6:c.350G>T
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ENSP00000218099.2:p.Cys117Phe
|
|
ENST00000394090.2:c.277+3762G>T
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ENSP00000377650.2:n.277+3762G>T
|
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ENST00000479617.2:n.303G>T
|
|
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NM_000133.3:c.350G>T , LRG_556t1:c.350G>T
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NP_000124.1:p.Cys117Phe
|
|
NM_001313913.1:c.277+3762G>T
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NP_001300842.1:n.277+3762G>T
|
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XM_005262397.3:c.350G>T
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XP_005262454.1:p.Cys117Phe
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XM_005262397.4:c.350G>T
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XP_005262454.1:p.Cys117Phe
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|
NM_000133.4:c.350G>T
MANE Select
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NP_000124.1:p.Cys117Phe
|
|
NM_001313913.2:c.277+3762G>T
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NP_001300842.1:n.277+3762G>T
|
|