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ENST00000314752.12:c.799A>G
MANE Select
|
ENSP00000321988.7:p.Thr267Ala
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ENST00000395607.6:c.*1451+2798A>G
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ENSP00000378971.2:n.*1451+2798A>G
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ENST00000395609.6:n.2432A>G
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ENST00000677940.1:c.139-12342A>G
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ENSP00000503077.1:n.139-12342A>G
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ENST00000679262.1:c.*118+14153A>G
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ENSP00000502863.1:n.*118+14153A>G
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ENST00000314752.11:c.799A>G
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ENSP00000321988.7:p.Thr267Ala
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ENST00000350842.8:c.565A>G
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ENSP00000329399.4:p.Thr189Ala
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ENST00000395607.5:c.799A>G
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ENSP00000378971.1:p.Thr267Ala
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ENST00000395609.5:c.799A>G
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ENSP00000378972.1:p.Thr267Ala
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|
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ENST00000562058.5:c.*1031A>G
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ENSP00000456215.1:n.*1031A>G
|
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ENST00000563493.1:c.*683A>G
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ENSP00000457083.1:n.*683A>G
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ENST00000564818.5:c.*1104A>G
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ENSP00000454388.1:n.*1104A>G
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ENST00000566189.5:c.799A>G
|
ENSP00000456459.1:p.Thr267Ala
|
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ENST00000567998.5:n.7629A>G
|
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ENST00000569554.5:c.799A>G
|
ENSP00000457912.1:p.Thr267Ala
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NM_001055.3:c.799A>G
|
NP_001046.2:p.Thr267Ala
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NM_177529.2:c.799A>G
|
NP_803565.1:p.Thr267Ala
|
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NM_177530.2:c.799A>G
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NP_803566.1:p.Thr267Ala
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NM_177534.2:c.799A>G
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NP_803878.1:p.Thr267Ala
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NM_177536.3:c.565A>G
|
NP_803880.1:p.Thr189Ala
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XM_017023604.1:c.817A>G
|
XP_016879093.1:p.Thr273Ala
|
|
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XM_017023605.1:c.817A>G
|
XP_016879094.1:p.Thr273Ala
|
|
|
XM_017023607.2:c.1072A>G
|
XP_016879096.1:p.Thr358Ala
|
|
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XM_017023608.1:c.817A>G
|
XP_016879097.1:p.Thr273Ala
|
|
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XM_017023609.1:c.817A>G
|
XP_016879098.1:p.Thr273Ala
|
|
|
XM_017023610.1:c.817A>G
|
XP_016879099.1:p.Thr273Ala
|
|
|
XM_017023611.2:c.799A>G
|
XP_016879100.1:p.Thr267Ala
|
|
|
XM_017023612.2:c.799A>G
|
XP_016879101.1:p.Thr267Ala
|
|
|
XM_017023613.2:c.799A>G
|
XP_016879102.1:p.Thr267Ala
|
|
|
XM_024450408.1:c.1075A>G
|
XP_024306176.1:p.Thr359Ala
|
|
|
XM_024450409.1:c.799A>G
|
XP_024306177.1:p.Thr267Ala
|
|
|
XM_024450410.1:c.799A>G
|
XP_024306178.1:p.Thr267Ala
|
|
|
XM_024450411.1:c.799A>G
|
XP_024306179.1:p.Thr267Ala
|
|
|
XR_001751973.1:n.1040A>G
|
|
|
|
NM_177530.3:c.799A>G
|
NP_803566.1:p.Thr267Ala
|
|
|
NM_177534.3:c.799A>G
|
NP_803878.1:p.Thr267Ala
|
|
|
NM_177536.4:c.565A>G
|
NP_803880.1:p.Thr189Ala
|
|
|
NM_001055.4:c.799A>G
MANE Select
|
NP_001046.2:p.Thr267Ala
|
|
|
NM_001394421.1:c.799A>G
|
NP_001381350.1:p.Thr267Ala
|
|
|
NM_001394422.1:c.799A>G
|
NP_001381351.1:p.Thr267Ala
|
|
|
NM_001394423.1:c.799A>G
|
NP_001381352.1:p.Thr267Ala
|
|
|
NM_001394424.1:c.799A>G
|
NP_001381353.1:p.Thr267Ala
|
|
|
NM_001394425.1:c.799A>G
|
NP_001381354.1:p.Thr267Ala
|
|
|
NM_177529.3:c.799A>G
|
NP_803565.1:p.Thr267Ala
|
|
|
NM_177530.4:c.799A>G
|
NP_803566.1:p.Thr267Ala
|
|
|
NM_177534.4:c.799A>G
|
NP_803878.1:p.Thr267Ala
|
|
|
NM_177536.5:c.496A>G
|
NP_803880.2:p.Thr166Ala
|
|
