ENST00000394867.9:n.1623C>A
|
|
|
ENST00000688002.1:n.3335C>A
|
|
|
ENST00000688751.1:n.320C>A
|
|
|
ENST00000689792.1:n.1088C>A
|
|
|
ENST00000262948.10:c.1184C>A
MANE Select
|
ENSP00000262948.4:p.Pro395His
|
|
ENST00000262948.9:c.1184C>A
|
ENSP00000262948.3:p.Pro395His
|
|
ENST00000394867.8:c.893C>A
|
ENSP00000378336.1:p.Pro298His
|
|
ENST00000597263.5:n.369C>A
|
|
|
ENST00000599021.1:c.294C>A
|
|
|
ENST00000600584.5:n.2633C>A
|
|
|
ENST00000601786.5:n.1485C>A
|
|
|
NM_030662.3:c.1184C>A , LRG_750t1:c.1184C>A
|
NP_109587.1:p.Pro395His
|
|
XM_006722799.2:c.905C>A
|
XP_006722862.1:p.Pro302His
|
|
XM_011528133.1:c.614C>A
|
XP_011526435.1:p.Pro205His
|
|
NM_030662.4:c.1184C>A
MANE Select
|
NP_109587.1:p.Pro395His
|
|