|
NM_000088.4:c.3509G>A
MANE Select
|
NP_000079.2:p.Arg1170His
|
|
ENST00000225964.10:c.3509G>A
MANE Select
|
ENSP00000225964.6:p.Arg1170His
|
|
NM_000088.3:c.3509G>A , LRG_1t1:c.3509G>A
|
NP_000079.2:p.Arg1170His
|
|
ENST00000225964.9:c.3509G>A
|
ENSP00000225964.5:p.Arg1170His
|
|
ENST00000510710.3:n.86G>A
|
|
|
XM_005257058.3:c.3239G>A
|
XP_005257115.2:p.Arg1080His
|
|
XM_005257058.4:c.3239G>A
|
XP_005257115.2:p.Arg1080His
|
|
XM_005257059.3:c.2591G>A
|
XP_005257116.2:p.Arg864His
|
|
XM_005257059.4:c.2591G>A
|
XP_005257116.2:p.Arg864His
|
|
XM_011524341.1:c.3311G>A
|
XP_011522643.1:p.Arg1104His
|