ENST00000225964.10:c.1731T>A
MANE Select
|
ENSP00000225964.6:p.Ala577=
|
|
ENST00000225964.9:c.1731T>A
|
ENSP00000225964.5:p.Ala577=
|
|
ENST00000463440.1:n.121T>A
|
|
|
ENST00000471344.1:n.763T>A
|
|
|
ENST00000476387.1:n.80T>A
|
|
|
NM_000088.3:c.1731T>A , LRG_1t1:c.1731T>A
|
NP_000079.2:p.Ala577=
|
|
XM_005257058.3:c.1731T>A
|
XP_005257115.2:p.Ala577=
|
|
XM_005257059.3:c.958-1286T>A
|
XP_005257116.2:n.958-1286T>A
|
|
XM_011524341.1:c.1533T>A
|
XP_011522643.1:p.Ala511=
|
|
XM_005257058.4:c.1731T>A
|
XP_005257115.2:p.Ala577=
|
|
XM_005257059.4:c.958-1286T>A
|
XP_005257116.2:n.958-1286T>A
|
|
NM_000088.4:c.1731T>A
MANE Select
|
NP_000079.2:p.Ala577=
|
|