ENST00000394867.9:n.1571G>C
|
|
|
ENST00000688002.1:n.3283G>C
|
|
|
ENST00000688751.1:n.268G>C
|
|
|
ENST00000689792.1:n.1036G>C
|
|
|
ENST00000262948.10:c.1132G>C
MANE Select
|
ENSP00000262948.4:p.Asp378His
|
|
ENST00000262948.9:c.1132G>C
|
ENSP00000262948.3:p.Asp378His
|
|
ENST00000394867.8:c.841G>C
|
ENSP00000378336.1:p.Asp281His
|
|
ENST00000597263.5:n.317G>C
|
|
|
ENST00000599021.1:c.242G>C
|
|
|
ENST00000600584.5:n.2581G>C
|
|
|
ENST00000601786.5:n.1433G>C
|
|
|
NM_030662.3:c.1132G>C , LRG_750t1:c.1132G>C
|
NP_109587.1:p.Asp378His
|
|
XM_006722799.2:c.853G>C
|
XP_006722862.1:p.Asp285His
|
|
XM_011528133.1:c.562G>C
|
XP_011526435.1:p.Asp188His
|
|
NM_030662.4:c.1132G>C
MANE Select
|
NP_109587.1:p.Asp378His
|
|