ENST00000291552.9:c.564C>G
MANE Select
|
ENSP00000291552.4:p.Arg188=
|
|
ENST00000291552.8:c.564C>G
|
ENSP00000291552.4:p.Arg188=
|
|
ENST00000380276.6:c.564C>G
|
ENSP00000369629.2:p.Arg188=
|
|
ENST00000398137.5:c.345C>G
|
ENSP00000381205.1:p.Arg115=
|
|
ENST00000459639.5:c.345C>G
|
ENSP00000418705.1:p.Arg115=
|
|
ENST00000464750.5:c.*403C>G
|
ENSP00000420672.1:n.*403C>G
|
|
ENST00000471250.5:n.1371C>G
|
|
|
ENST00000475639.5:n.4389C>G
|
|
|
ENST00000478282.1:n.1818C>G
|
|
|
ENST00000486519.5:n.611C>G
|
|
|
NM_001025203.1:c.564C>G , LRG_615t1:c.564C>G
|
NP_001020374.1:p.Arg188=
|
|
NM_001025204.1:c.345C>G
|
NP_001020375.1:p.Arg115=
|
|
NM_006758.2:c.564C>G , LRG_615t2:c.564C>G
|
NP_006749.1:p.Arg188=
|
|
XM_011529743.1:c.465C>G
|
XP_011528045.1:p.Arg155=
|
|
XM_011529743.3:c.465C>G
|
XP_011528045.1:p.Arg155=
|
|
XM_017028468.2:c.465C>G
|
XP_016883957.1:p.Arg155=
|
|
XM_024452129.1:c.345C>G
|
XP_024307897.1:p.Arg115=
|
|
XM_024452130.1:c.345C>G
|
XP_024307898.1:p.Arg115=
|
|
XM_024452131.1:c.345C>G
|
XP_024307899.1:p.Arg115=
|
|
NM_001025204.2:c.345C>G
|
NP_001020375.1:p.Arg115=
|
|
NM_006758.3:c.564C>G
MANE Select
|
NP_006749.1:p.Arg188=
|
|