ENST00000452035.7:n.2095G>T
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ENST00000483004.2:c.1487G>T
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ENSP00000419887.2:p.Gly496Val
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ENST00000698628.1:c.1624+294G>T
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ENSP00000513848.1:n.1624+294G>T
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ENST00000698629.1:n.1880G>T
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ENST00000698630.1:n.2419G>T
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ENST00000698631.1:n.2420G>T
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ENST00000698632.1:n.3214G>T
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ENST00000698633.1:n.3104G>T
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ENST00000698636.1:n.1925G>T
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ENST00000425368.7:c.1703G>T
MANE Select
|
ENSP00000416561.2:p.Gly568Val
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ENST00000425368.6:c.1703G>T
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ENSP00000416561.2:p.Gly568Val
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ENST00000456570.5:c.3209G>T
|
ENSP00000410815.1:p.Gly1070Val
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ENST00000467360.1:n.829G>T
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ENST00000477310.1:c.2756G>T
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ENSP00000418996.1:p.Gly919Val
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ENST00000483004.1:c.325G>T
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|
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NM_001710.5:c.1703G>T , LRG_136t1:c.1703G>T
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NP_001701.2:p.Gly568Val
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NM_001710.6:c.1703G>T
MANE Select
|
NP_001701.2:p.Gly568Val
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