ENST00000452035.7:n.2169A>G
|
|
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ENST00000483004.2:c.1561A>G
|
ENSP00000419887.2:p.Arg521Gly
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|
ENST00000698628.1:c.1624+368A>G
|
ENSP00000513848.1:n.1624+368A>G
|
|
ENST00000698629.1:n.1954A>G
|
|
|
ENST00000698630.1:n.2493A>G
|
|
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ENST00000698631.1:n.2494A>G
|
|
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ENST00000698632.1:n.3288A>G
|
|
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ENST00000698633.1:n.3178A>G
|
|
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ENST00000698636.1:n.1999A>G
|
|
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ENST00000425368.7:c.1777A>G
MANE Select
|
ENSP00000416561.2:p.Arg593Gly
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|
ENST00000425368.6:c.1777A>G
|
ENSP00000416561.2:p.Arg593Gly
|
|
ENST00000456570.5:c.3283A>G
|
ENSP00000410815.1:p.Arg1095Gly
|
|
ENST00000467360.1:n.903A>G
|
|
|
ENST00000477310.1:c.2830A>G
|
ENSP00000418996.1:p.Arg944Gly
|
|
ENST00000483004.1:c.399A>G
|
|
|
NM_001710.5:c.1777A>G , LRG_136t1:c.1777A>G
|
NP_001701.2:p.Arg593Gly
|
|
NM_001710.6:c.1777A>G
MANE Select
|
NP_001701.2:p.Arg593Gly
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