ENST00000321612.8:c.2097C>A
MANE Select
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ENSP00000370737.4:p.Tyr699Ter
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ENST00000638233.1:n.532C>A
|
|
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ENST00000638661.1:c.297C>A
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ENSP00000491369.1:p.Tyr99Ter
|
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ENST00000638694.1:n.284C>A
|
|
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ENST00000639318.1:c.297C>A
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ENSP00000491932.1:p.Tyr99Ter
|
|
ENST00000639364.1:n.1797C>A
|
|
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ENST00000639443.1:n.1665C>A
|
|
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ENST00000639954.1:n.1805C>A
|
|
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ENST00000640505.1:n.336C>A
|
|
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ENST00000321612.6:c.2097C>A
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ENSP00000370737.3:p.Tyr699Ter
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NM_000170.2:c.2097C>A , LRG_643t1:c.2097C>A
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NP_000161.2:p.Tyr699Ter
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NM_000170.3:c.2097C>A
MANE Select
|
NP_000161.2:p.Tyr699Ter
|
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