ENST00000321612.8:c.2142T>C
MANE Select
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ENSP00000370737.4:p.Cys714=
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ENST00000638233.1:n.577T>C
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ENST00000638661.1:c.342T>C
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ENSP00000491369.1:p.Cys114=
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ENST00000638694.1:n.329T>C
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|
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ENST00000639318.1:c.342T>C
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ENSP00000491932.1:p.Cys114=
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ENST00000639364.1:n.1842T>C
|
|
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ENST00000639443.1:n.1710T>C
|
|
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ENST00000639954.1:n.1850T>C
|
|
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ENST00000640505.1:n.381T>C
|
|
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ENST00000321612.6:c.2142T>C
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ENSP00000370737.3:p.Cys714=
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NM_000170.2:c.2142T>C , LRG_643t1:c.2142T>C
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NP_000161.2:p.Cys714=
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NM_000170.3:c.2142T>C
MANE Select
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NP_000161.2:p.Cys714=
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