ENST00000477226.6:n.870C>T
|
|
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ENST00000683013.1:n.784C>T
|
|
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ENST00000373960.4:c.1396C>T
MANE Select
|
ENSP00000363071.3:p.Gln466Ter
|
|
ENST00000373960.3:c.1396C>T
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ENSP00000363071.3:p.Gln466Ter
|
|
ENST00000483395.1:n.251C>T
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|
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NM_001927.3:c.1396C>T , LRG_380t1:c.1396C>T
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NP_001918.3:p.Gln466Ter
|
|
NM_001927.4:c.1396C>T
MANE Select
|
NP_001918.3:p.Gln466Ter
|
|
NM_001382708.1:c.1393C>T
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NP_001369637.1:p.Gln465Ter
|
|
NM_001382709.1:c.964C>T
|
NP_001369638.1:p.Gln322Ter
|
|
NM_001382710.1:c.1327C>T
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NP_001369639.1:p.Gln443Ter
|
|
NM_001382711.1:c.1375C>T
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NP_001369640.1:p.Gln459Ter
|
|
NM_001382712.1:c.1371+228C>T
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NP_001369641.1:n.1371+228C>T
|
|
NM_001382713.1:c.1126C>T
|
NP_001369642.1:p.Gln376Ter
|
|