ENST00000309383.6:c.2102G>A
MANE Select
|
ENSP00000310649.1:p.Arg701Gln
|
|
ENST00000309383.5:c.2102G>A
|
ENSP00000310649.1:p.Arg701Gln
|
|
ENST00000326848.7:c.1187G>A
|
ENSP00000320853.7:p.Arg396Gln
|
|
ENST00000590333.5:c.2150G>A
|
ENSP00000468190.1:p.Arg717Gln
|
|
NM_032430.1:c.2102G>A
|
NP_115806.1:p.Arg701Gln
|
|
XM_005259327.2:c.1832G>A
|
XP_005259384.1:p.Arg611Gln
|
|
XM_011527395.1:c.1859G>A
|
XP_011525697.1:p.Arg620Gln
|
|
XR_430213.2:n.2085G>A
|
|
|
XM_005259327.3:c.1832G>A
|
XP_005259384.1:p.Arg611Gln
|
|
XM_011527395.2:c.1574G>A
|
XP_011525697.2:p.Arg525Gln
|
|
XM_024451739.1:c.1877G>A
|
XP_024307507.1:p.Arg626Gln
|
|
XR_430213.4:n.2383G>A
|
|
|
NM_032430.2:c.2102G>A
MANE Select
|
NP_115806.1:p.Arg701Gln
|
|