ENST00000321612.8:c.2052+33C>A
MANE Select
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ENSP00000370737.4:n.2052+33C>A
|
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ENST00000460457.2:n.212+33C>A
|
|
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ENST00000638233.1:n.487+33C>A
|
|
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ENST00000638661.1:c.252+33C>A
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ENSP00000491369.1:n.252+33C>A
|
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ENST00000638694.1:n.239+33C>A
|
|
|
ENST00000639318.1:c.252+33C>A
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ENSP00000491932.1:n.252+33C>A
|
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ENST00000639364.1:n.1752+33C>A
|
|
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ENST00000639443.1:n.1620+33C>A
|
|
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ENST00000639954.1:n.1760+33C>A
|
|
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ENST00000640208.1:c.285C>A
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ENSP00000491895.1:p.Gly95=
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ENST00000640505.1:n.291+33C>A
|
|
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ENST00000640592.1:n.1968C>A
|
|
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ENST00000321612.6:c.2052+33C>A
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ENSP00000370737.3:n.2052+33C>A
|
|
ENST00000460457.1:n.224C>A
|
|
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NM_000170.2:c.2052+33C>A , LRG_643t1:c.2052+33C>A
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NP_000161.2:n.2052+33C>A
|
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NM_000170.3:c.2052+33C>A
MANE Select
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NP_000161.2:n.2052+33C>A
|
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