ENST00000308736.7:c.3302G>A
MANE Select
|
ENSP00000311135.2:p.Arg1101His
|
|
ENST00000544745.2:c.2773G>A
|
|
|
ENST00000308736.6:c.3302G>A
|
ENSP00000311135.2:p.Arg1101His
|
|
ENST00000507267.2:n.446G>A
|
|
|
ENST00000539298.1:n.3402G>A
|
|
|
ENST00000542400.5:n.1916G>A
|
|
|
ENST00000544745.1:c.2663G>A
|
ENSP00000439009.1:p.Arg888His
|
|
NM_032656.3:c.3302G>A
|
NP_116045.2:p.Arg1101His
|
|
XM_005253590.2:c.3302G>A
|
XP_005253647.1:p.Arg1101His
|
|
XM_005253590.3:c.3302G>A
|
XP_005253647.1:p.Arg1101His
|
|
XR_001748819.1:n.3442G>A
|
|
|
XR_001748820.1:n.3395G>A
|
|
|
NM_032656.4:c.3302G>A
MANE Select
|
NP_116045.2:p.Arg1101His
|
|