ENST00000452035.7:n.2305T>G
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|
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ENST00000483004.2:c.1602T>G
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ENSP00000419887.2:p.Ala534=
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ENST00000698628.1:c.1625-237T>G
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ENSP00000513848.1:n.1625-237T>G
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ENST00000698629.1:n.2090T>G
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|
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ENST00000698630.1:n.2534T>G
|
|
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ENST00000698631.1:n.2535T>G
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|
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ENST00000698632.1:n.3424T>G
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|
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ENST00000698633.1:n.3314T>G
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|
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ENST00000425368.7:c.1818T>G
MANE Select
|
ENSP00000416561.2:p.Ala606=
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ENST00000425368.6:c.1818T>G
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ENSP00000416561.2:p.Ala606=
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ENST00000456570.5:c.3324T>G
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ENSP00000410815.1:p.Ala1108=
|
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ENST00000467360.1:n.944T>G
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|
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ENST00000477310.1:c.2871T>G
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ENSP00000418996.1:p.Ala957=
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ENST00000482312.1:n.34T>G
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|
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ENST00000483004.1:c.440T>G
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|
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NM_001710.5:c.1818T>G , LRG_136t1:c.1818T>G
|
NP_001701.2:p.Ala606=
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NM_001710.6:c.1818T>G
MANE Select
|
NP_001701.2:p.Ala606=
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