ENST00000452035.7:n.1791G>T
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|
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ENST00000483004.2:c.1409-226G>T
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ENSP00000419887.2:n.1409-226G>T
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|
ENST00000698628.1:c.1614G>T
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ENSP00000513848.1:p.Lys538Asn
|
|
ENST00000698629.1:n.1791G>T
|
|
|
ENST00000698630.1:n.2330G>T
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|
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ENST00000698631.1:n.2331G>T
|
|
|
ENST00000698632.1:n.2910G>T
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|
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ENST00000698633.1:n.2800G>T
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|
|
ENST00000698636.1:n.1836G>T
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|
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ENST00000425368.7:c.1614G>T
MANE Select
|
ENSP00000416561.2:p.Lys538Asn
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|
ENST00000425368.6:c.1614G>T
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ENSP00000416561.2:p.Lys538Asn
|
|
ENST00000452035.6:n.1614G>T
|
|
|
ENST00000456570.5:c.3120G>T
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ENSP00000410815.1:p.Lys1040Asn
|
|
ENST00000467360.1:n.525G>T
|
|
|
ENST00000477310.1:c.2667G>T
|
ENSP00000418996.1:p.Lys889Asn
|
|
ENST00000483004.1:c.247-226G>T
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|
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NM_001710.5:c.1614G>T , LRG_136t1:c.1614G>T
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NP_001701.2:p.Lys538Asn
|
|
NM_001710.6:c.1614G>T
MANE Select
|
NP_001701.2:p.Lys538Asn
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