ENST00000394867.9:n.1604C>G
|
|
|
ENST00000688002.1:n.3316C>G
|
|
|
ENST00000688751.1:n.301C>G
|
|
|
ENST00000689792.1:n.1069C>G
|
|
|
ENST00000262948.10:c.1165C>G
MANE Select
|
ENSP00000262948.4:p.Leu389Val
|
|
ENST00000262948.9:c.1165C>G
|
ENSP00000262948.3:p.Leu389Val
|
|
ENST00000394867.8:c.874C>G
|
ENSP00000378336.1:p.Leu292Val
|
|
ENST00000597263.5:n.350C>G
|
|
|
ENST00000599021.1:c.275C>G
|
|
|
ENST00000600584.5:n.2614C>G
|
|
|
ENST00000601786.5:n.1466C>G
|
|
|
NM_030662.3:c.1165C>G , LRG_750t1:c.1165C>G
|
NP_109587.1:p.Leu389Val
|
|
XM_006722799.2:c.886C>G
|
XP_006722862.1:p.Leu296Val
|
|
XM_011528133.1:c.595C>G
|
XP_011526435.1:p.Leu199Val
|
|
NM_030662.4:c.1165C>G
MANE Select
|
NP_109587.1:p.Leu389Val
|
|