ENST00000684241.1:n.3404G>A
|
|
|
ENST00000262186.10:c.2571G>A
MANE Select
|
ENSP00000262186.5:p.Glu857=
|
|
ENST00000330883.9:c.1551G>A
|
ENSP00000328531.4:p.Glu517=
|
|
ENST00000262186.9:c.2571G>A
|
ENSP00000262186.5:p.Glu857=
|
|
ENST00000330883.8:c.1551G>A
|
ENSP00000328531.4:p.Glu517=
|
|
NM_000238.3:c.2571G>A , LRG_288t1:c.2571G>A
|
NP_000229.1:p.Glu857=
|
|
NM_172057.2:c.1551G>A , LRG_288t3:c.1551G>A
|
NP_742054.1:p.Glu517=
|
|
XM_011516185.1:c.2271G>A
|
XP_011514487.1:p.Glu757=
|
|
XM_011516186.1:c.2571G>A
|
XP_011514488.1:p.Glu857=
|
|
XM_011516185.2:c.2271G>A
|
XP_011514487.1:p.Glu757=
|
|
XM_011516186.3:c.2571G>A
|
XP_011514488.1:p.Glu857=
|
|
XM_017012195.1:c.2421G>A
|
XP_016867684.1:p.Glu807=
|
|
XM_017012196.1:c.2394G>A
|
XP_016867685.1:p.Glu798=
|
|
NM_000238.4:c.2571G>A
MANE Select
|
NP_000229.1:p.Glu857=
|
|
NM_172057.3:c.1551G>A
|
NP_742054.1:p.Glu517=
|
|