ENST00000477226.6:n.875T>A
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|
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ENST00000683013.1:n.789T>A
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|
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ENST00000373960.4:c.1401T>A
MANE Select
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ENSP00000363071.3:p.His467Gln
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ENST00000373960.3:c.1401T>A
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ENSP00000363071.3:p.His467Gln
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ENST00000483395.1:n.256T>A
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NM_001927.3:c.1401T>A , LRG_380t1:c.1401T>A
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NP_001918.3:p.His467Gln
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NM_001927.4:c.1401T>A
MANE Select
|
NP_001918.3:p.His467Gln
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NM_001382708.1:c.1398T>A
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NP_001369637.1:p.His466Gln
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NM_001382709.1:c.969T>A
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NP_001369638.1:p.His323Gln
|
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NM_001382710.1:c.1332T>A
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NP_001369639.1:p.His444Gln
|
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NM_001382711.1:c.1380T>A
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NP_001369640.1:p.His460Gln
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NM_001382712.1:c.1371+233T>A
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NP_001369641.1:n.1371+233T>A
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NM_001382713.1:c.1131T>A
|
NP_001369642.1:p.His377Gln
|
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