ENST00000480266.6:c.1099T=
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ENSP00000479015.1:p.Cys367=
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|
ENST00000373203.9:c.1645T=
MANE Select
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ENSP00000362299.4:p.Cys549=
|
|
ENST00000344849.4:c.1645T=
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ENSP00000341917.3:p.Cys549=
|
|
ENST00000373203.8:c.1645T=
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ENSP00000362299.4:p.Cys549=
|
|
ENST00000480266.5:c.1099T=
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ENSP00000479015.1:p.Cys367=
|
|
NM_000118.3:c.1645T= , LRG_589t1:c.1645T=
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NP_000109.1:p.Cys549=
|
|
NM_001114753.2:c.1645T= , LRG_589t2:c.1645T=
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NP_001108225.1:p.Cys549=
|
|
NM_001278138.1:c.1099T=
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NP_001265067.1:p.Cys367=
|
|
NR_136302.1:n.1378-150A=
|
|
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NM_001114753.3:c.1645T=
MANE Select
|
NP_001108225.1:p.Cys549=
|
|
NM_001278138.2:c.1099T=
|
NP_001265067.1:p.Cys367=
|
|