ENST00000525403.6:c.1012G>A
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ENSP00000432210.2:p.Ala338Thr
|
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ENST00000533343.2:n.1833G>A
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|
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ENST00000698909.1:n.1811G>A
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|
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ENST00000698910.1:c.745G>A
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ENSP00000514024.1:p.Ala249Thr
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ENST00000698911.1:c.1012G>A
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ENSP00000514025.1:p.Ala338Thr
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ENST00000698912.1:c.1012G>A
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ENSP00000514026.1:p.Ala338Thr
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ENST00000698913.1:c.1012G>A
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ENSP00000514027.1:p.Ala338Thr
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ENST00000698915.1:c.1234G>A
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ENSP00000514029.1:p.Ala412Thr
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ENST00000698916.1:c.1255G>A
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ENSP00000514030.1:p.Ala419Thr
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ENST00000698918.1:c.*935G>A
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ENSP00000514031.1:n.*935G>A
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ENST00000698919.1:c.*167G>A
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ENSP00000514032.1:n.*167G>A
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ENST00000698920.1:n.534G>A
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ENST00000526596.2:c.1234G>A
MANE Select
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ENSP00000433266.2:p.Ala412Thr
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ENST00000300737.8:c.1234G>A
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ENSP00000300737.4:p.Ala412Thr
|
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ENST00000526596.1:c.426G>A
|
|
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ENST00000527651.5:c.1234G>A
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ENSP00000436208.1:p.Ala412Thr
|
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ENST00000533343.1:n.244G>A
|
|
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ENST00000533977.5:c.715G>A
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ENSP00000434767.1:p.Ala239Thr
|
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ENST00000616714.4:c.1234G>A
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ENSP00000478059.1:p.Ala412Thr
|
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NM_001277961.1:c.1234G>A
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NP_001264890.1:p.Ala412Thr
|
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NM_001277962.1:c.1234G>A
|
NP_001264891.1:p.Ala412Thr
|
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NM_003156.3:c.1234G>A , LRG_164t1:c.1234G>A
|
NP_003147.2:p.Ala412Thr
|
|
NM_001277962.2:c.1234G>A
|
NP_001264891.1:p.Ala412Thr
|
|
NM_001277961.3:c.1234G>A
|
NP_001264890.1:p.Ala412Thr
|
|
NM_001382566.1:c.1012G>A
|
NP_001369495.1:p.Ala338Thr
|
|
NM_001382567.1:c.1234G>A
MANE Select
|
NP_001369496.1:p.Ala412Thr
|
|
NM_001382568.1:c.1234G>A
|
NP_001369497.1:p.Ala412Thr
|
|
NM_001382569.1:c.1099G>A
|
NP_001369498.1:p.Ala367Thr
|
|
NM_001382570.1:c.1006G>A
|
NP_001369499.1:p.Ala336Thr
|
|
NM_001382571.1:c.754G>A
|
NP_001369500.1:p.Ala252Thr
|
|
NM_001382573.1:c.1012G>A
|
NP_001369502.1:p.Ala338Thr
|
|
NM_001382575.1:c.1012G>A
|
NP_001369504.1:p.Ala338Thr
|
|
NM_001382576.1:c.1012G>A
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NP_001369505.1:p.Ala338Thr
|
|
NM_001382577.1:c.1012G>A
|
NP_001369506.1:p.Ala338Thr
|
|
NM_001382578.1:c.1012G>A
|
NP_001369507.1:p.Ala338Thr
|
|
NM_001382579.1:c.1012G>A
|
NP_001369508.1:p.Ala338Thr
|
|
NM_001382580.1:c.745G>A
|
NP_001369509.1:p.Ala249Thr
|
|
NM_001382581.1:c.745G>A
|
NP_001369510.1:p.Ala249Thr
|
|
NM_003156.4:c.1234G>A
|
NP_003147.2:p.Ala412Thr
|
|
NR_168436.1:n.1399-3499G>A
|
|
|
NR_168437.1:n.1663G>A
|
|
|
NR_168438.1:n.1485G>A
|
|
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