ENST00000264638.9:c.1062T>G
MANE Select
|
ENSP00000264638.3:p.Arg354=
|
|
ENST00000264638.8:c.1062T>G
|
ENSP00000264638.3:p.Arg354=
|
|
ENST00000586801.1:n.477T>G
|
|
|
ENST00000591662.1:c.1062T>G
|
ENSP00000466571.1:p.Arg354=
|
|
NM_003632.2:c.1062T>G
|
NP_003623.1:p.Arg354=
|
|
XM_005257748.3:c.834T>G
|
XP_005257805.1:p.Arg278=
|
|
XM_005257748.4:c.834T>G
|
XP_005257805.1:p.Arg278=
|
|
XM_017025238.1:c.1062T>G
|
XP_016880727.1:p.Arg354=
|
|
XM_024451011.1:c.1062T>G
|
XP_024306779.1:p.Arg354=
|
|
NM_003632.3:c.1062T>G
MANE Select
|
NP_003623.1:p.Arg354=
|
|