ENST00000452035.7:n.2074T>A
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|
|
ENST00000483004.2:c.1466T>A
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ENSP00000419887.2:p.Ile489Asn
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|
ENST00000698628.1:c.1624+273T>A
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ENSP00000513848.1:n.1624+273T>A
|
|
ENST00000698629.1:n.1859T>A
|
|
|
ENST00000698630.1:n.2398T>A
|
|
|
ENST00000698631.1:n.2399T>A
|
|
|
ENST00000698632.1:n.3193T>A
|
|
|
ENST00000698633.1:n.3083T>A
|
|
|
ENST00000698636.1:n.1904T>A
|
|
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ENST00000425368.7:c.1682T>A
MANE Select
|
ENSP00000416561.2:p.Ile561Asn
|
|
ENST00000425368.6:c.1682T>A
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ENSP00000416561.2:p.Ile561Asn
|
|
ENST00000456570.5:c.3188T>A
|
ENSP00000410815.1:p.Ile1063Asn
|
|
ENST00000467360.1:n.808T>A
|
|
|
ENST00000477310.1:c.2735T>A
|
ENSP00000418996.1:p.Ile912Asn
|
|
ENST00000483004.1:c.304T>A
|
|
|
NM_001710.5:c.1682T>A , LRG_136t1:c.1682T>A
|
NP_001701.2:p.Ile561Asn
|
|
NM_001710.6:c.1682T>A
MANE Select
|
NP_001701.2:p.Ile561Asn
|
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