ENST00000477226.6:n.855G>T
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|
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ENST00000683013.1:n.769G>T
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|
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ENST00000373960.4:c.1381G>T
MANE Select
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ENSP00000363071.3:p.Glu461Ter
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ENST00000373960.3:c.1381G>T
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ENSP00000363071.3:p.Glu461Ter
|
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ENST00000483395.1:n.236G>T
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NM_001927.3:c.1381G>T , LRG_380t1:c.1381G>T
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NP_001918.3:p.Glu461Ter
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|
NM_001927.4:c.1381G>T
MANE Select
|
NP_001918.3:p.Glu461Ter
|
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NM_001382708.1:c.1378G>T
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NP_001369637.1:p.Glu460Ter
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NM_001382709.1:c.949G>T
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NP_001369638.1:p.Glu317Ter
|
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NM_001382710.1:c.1312G>T
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NP_001369639.1:p.Glu438Ter
|
|
NM_001382711.1:c.1360G>T
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NP_001369640.1:p.Glu454Ter
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NM_001382712.1:c.1371+213G>T
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NP_001369641.1:n.1371+213G>T
|
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NM_001382713.1:c.1111G>T
|
NP_001369642.1:p.Glu371Ter
|
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