ENST00000477226.6:n.882C>G
|
|
|
ENST00000683013.1:n.796C>G
|
|
|
ENST00000373960.4:c.1408C>G
MANE Select
|
ENSP00000363071.3:p.Leu470Val
|
|
ENST00000373960.3:c.1408C>G
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ENSP00000363071.3:p.Leu470Val
|
|
ENST00000483395.1:n.263C>G
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|
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NM_001927.3:c.1408C>G , LRG_380t1:c.1408C>G
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NP_001918.3:p.Leu470Val
|
|
NM_001927.4:c.1408C>G
MANE Select
|
NP_001918.3:p.Leu470Val
|
|
NM_001382708.1:c.1405C>G
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NP_001369637.1:p.Leu469Val
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|
NM_001382709.1:c.976C>G
|
NP_001369638.1:p.Leu326Val
|
|
NM_001382710.1:c.1339C>G
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NP_001369639.1:p.Leu447Val
|
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NM_001382711.1:c.1387C>G
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NP_001369640.1:p.Leu463Val
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NM_001382712.1:c.1371+240C>G
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NP_001369641.1:n.1371+240C>G
|
|
NM_001382713.1:c.1138C>G
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NP_001369642.1:p.Leu380Val
|
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