ENST00000477226.6:n.883T>A
|
|
|
ENST00000683013.1:n.797T>A
|
|
|
ENST00000373960.4:c.1409T>A
MANE Select
|
ENSP00000363071.3:p.Leu470His
|
|
ENST00000373960.3:c.1409T>A
|
ENSP00000363071.3:p.Leu470His
|
|
ENST00000483395.1:n.264T>A
|
|
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NM_001927.3:c.1409T>A , LRG_380t1:c.1409T>A
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NP_001918.3:p.Leu470His
|
|
NM_001927.4:c.1409T>A
MANE Select
|
NP_001918.3:p.Leu470His
|
|
NM_001382708.1:c.1406T>A
|
NP_001369637.1:p.Leu469His
|
|
NM_001382709.1:c.977T>A
|
NP_001369638.1:p.Leu326His
|
|
NM_001382710.1:c.1340T>A
|
NP_001369639.1:p.Leu447His
|
|
NM_001382711.1:c.1388T>A
|
NP_001369640.1:p.Leu463His
|
|
NM_001382712.1:c.1371+241T>A
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NP_001369641.1:n.1371+241T>A
|
|
NM_001382713.1:c.1139T>A
|
NP_001369642.1:p.Leu380His
|
|