NM_173602.3:c.1632G>A
MANE Select
|
NP_775873.2:p.Ser544=
|
ENST00000301180.10:c.1632G>A
MANE Select
|
ENSP00000301180.5:p.Ser544=
|
NM_173602.2:c.1632G>A
|
NP_775873.2:p.Ser544=
|
ENST00000301180.9:c.1632G>A
|
ENSP00000301180.5:p.Ser544=
|
ENST00000546732.1:c.182-1820G>A
|
|
XM_005269044.1:c.1635G>A
|
XP_005269101.1:p.Ser545=
|
XM_006719520.2:c.1662G>A
|
XP_006719583.1:p.Ser554=
|
XM_006719521.2:c.1449G>A
|
XP_006719584.1:p.Ser483=
|
XM_006719522.2:c.1281G>A
|
XP_006719585.1:p.Ser427=
|
XM_011538594.1:c.1665G>A
|
XP_011536896.1:p.Ser555=
|
XM_011538595.1:c.1585-4138G>A
|
XP_011536897.1:n.1585-4138G>A
|
XM_011538596.1:c.1452G>A
|
XP_011536898.1:p.Ser484=
|