ENST00000261769.10:c.2261A>G
MANE Select
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ENSP00000261769.4:p.Tyr754Cys
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|
ENST00000261769.9:c.2261A>G
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ENSP00000261769.4:p.Tyr754Cys
|
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ENST00000422392.6:c.2078A>G
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ENSP00000414946.2:p.Tyr693Cys
|
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ENST00000562118.1:n.479A>G
|
|
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ENST00000562836.5:n.2332A>G
|
|
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ENST00000566510.5:c.*927A>G
|
ENSP00000458139.1:n.*927A>G
|
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ENST00000566612.5:c.*501A>G
|
ENSP00000454782.1:n.*501A>G
|
|
ENST00000611625.4:c.2324A>G
|
ENSP00000481063.1:p.Tyr775Cys
|
|
ENST00000612417.4:c.1853+1716A>G
|
ENSP00000478360.1:n.1853+1716A>G
|
|
ENST00000621016.4:c.1866-5933A>G
|
ENSP00000480664.1:n.1866-5933A>G
|
|
NM_004360.3:c.2261A>G , LRG_301t1:c.2261A>G
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NP_004351.1:p.Tyr754Cys
|
|
XM_011523488.1:c.1526A>G
|
XP_011521790.1:p.Tyr509Cys
|
|
XM_011523489.1:c.1526A>G
|
XP_011521791.1:p.Tyr509Cys
|
|
NM_001317184.1:c.2078A>G
|
NP_001304113.1:p.Tyr693Cys
|
|
NM_001317185.1:c.713A>G
|
NP_001304114.1:p.Tyr238Cys
|
|
NM_001317186.1:c.296A>G
|
NP_001304115.1:p.Tyr99Cys
|
|
NM_004360.4:c.2261A>G
|
NP_004351.1:p.Tyr754Cys
|
|
NM_004360.5:c.2261A>G
MANE Select
|
NP_004351.1:p.Tyr754Cys
|
|
NM_001317184.2:c.2078A>G
|
NP_001304113.1:p.Tyr693Cys
|
|
NM_001317185.2:c.713A>G
|
NP_001304114.1:p.Tyr238Cys
|
|
NM_001317186.2:c.296A>G
|
NP_001304115.1:p.Tyr99Cys
|
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