ENST00000394867.9:n.1434A>G
|
|
|
ENST00000688002.1:n.3146A>G
|
|
|
ENST00000688751.1:n.131A>G
|
|
|
ENST00000689792.1:n.899A>G
|
|
|
ENST00000262948.10:c.995A>G
MANE Select
|
ENSP00000262948.4:p.Lys332Arg
|
|
ENST00000262948.9:c.995A>G
|
ENSP00000262948.3:p.Lys332Arg
|
|
ENST00000394867.8:c.704A>G
|
ENSP00000378336.1:p.Lys235Arg
|
|
ENST00000595715.1:n.810A>G
|
|
|
ENST00000597263.5:n.180A>G
|
|
|
ENST00000599021.1:c.105A>G
|
|
|
ENST00000600584.5:n.1555A>G
|
|
|
ENST00000601786.5:n.1296A>G
|
|
|
NM_030662.3:c.995A>G , LRG_750t1:c.995A>G
|
NP_109587.1:p.Lys332Arg
|
|
XM_006722799.2:c.716A>G
|
XP_006722862.1:p.Lys239Arg
|
|
XM_011528133.1:c.425A>G
|
XP_011526435.1:p.Lys142Arg
|
|
XM_017026989.1:c.995A>G
|
XP_016882478.1:p.Lys332Arg
|
|
XM_017026990.1:c.716A>G
|
XP_016882479.1:p.Lys239Arg
|
|
NM_030662.4:c.995A>G
MANE Select
|
NP_109587.1:p.Lys332Arg
|
|