ENST00000321612.8:c.1986C>T
MANE Select
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ENSP00000370737.4:p.Gly662=
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ENST00000460457.2:n.146C>T
|
|
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ENST00000638233.1:n.421C>T
|
|
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ENST00000638661.1:c.186C>T
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ENSP00000491369.1:p.Gly62=
|
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ENST00000638694.1:n.173C>T
|
|
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ENST00000639318.1:c.186C>T
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ENSP00000491932.1:p.Gly62=
|
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ENST00000639364.1:n.1686C>T
|
|
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ENST00000639443.1:n.1554C>T
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|
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ENST00000639954.1:n.1694C>T
|
|
|
ENST00000640208.1:c.186C>T
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ENSP00000491895.1:p.Gly62=
|
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ENST00000640505.1:n.225C>T
|
|
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ENST00000640592.1:n.1869C>T
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|
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ENST00000321612.6:c.1986C>T
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ENSP00000370737.3:p.Gly662=
|
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ENST00000460457.1:n.125C>T
|
|
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NM_000170.2:c.1986C>T , LRG_643t1:c.1986C>T
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NP_000161.2:p.Gly662=
|
|
NM_000170.3:c.1986C>T
MANE Select
|
NP_000161.2:p.Gly662=
|
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