ENST00000308736.7:c.1460G>A
MANE Select
|
ENSP00000311135.2:p.Arg487His
|
|
ENST00000544745.2:c.931G>A
|
|
|
ENST00000679875.1:n.1532G>A
|
|
|
ENST00000308736.6:c.1460G>A
|
ENSP00000311135.2:p.Arg487His
|
|
ENST00000539298.1:n.1560G>A
|
|
|
ENST00000544745.1:c.821G>A
|
ENSP00000439009.1:p.Arg274His
|
|
NM_032656.3:c.1460G>A
|
NP_116045.2:p.Arg487His
|
|
XM_005253590.2:c.1460G>A
|
XP_005253647.1:p.Arg487His
|
|
XM_011538597.1:c.1460G>A
|
XP_011536899.1:p.Arg487His
|
|
XM_011538598.1:c.1460G>A
|
XP_011536900.1:p.Arg487His
|
|
XM_011538599.1:c.1460G>A
|
XP_011536901.1:p.Arg487His
|
|
XM_011538600.1:c.1460G>A
|
XP_011536902.1:p.Arg487His
|
|
XM_005253590.3:c.1460G>A
|
XP_005253647.1:p.Arg487His
|
|
XM_011538598.2:c.1460G>A
|
XP_011536900.1:p.Arg487His
|
|
XM_011538600.2:c.1460G>A
|
XP_011536902.1:p.Arg487His
|
|
XR_001748819.1:n.1563G>A
|
|
|
XR_001748820.1:n.1563G>A
|
|
|
NM_032656.4:c.1460G>A
MANE Select
|
NP_116045.2:p.Arg487His
|
|