ENST00000270357.10:c.1572T>A
MANE Select
|
ENSP00000270357.4:p.Ser524=
|
|
ENST00000270357.8:c.879T>A
|
ENSP00000270357.3:p.Ser293=
|
|
ENST00000437406.1:c.138T>A
|
ENSP00000403319.1:p.Ser46=
|
|
ENST00000451363.5:c.213T>A
|
ENSP00000414661.1:p.Ser71=
|
|
ENST00000464550.5:n.408T>A
|
|
|
ENST00000471657.1:n.375T>A
|
|
|
ENST00000481757.5:n.2506T>A
|
|
|
ENST00000486058.5:n.1685T>A
|
|
|
ENST00000493398.5:n.718T>A
|
|
|
NM_018226.4:c.1572T>A
|
NP_060696.4:p.Ser524=
|
|
XM_005247036.3:c.1539T>A
|
XP_005247093.1:p.Ser513=
|
|
NM_018226.5:c.1572T>A
|
NP_060696.4:p.Ser524=
|
|
XM_005247036.4:c.1539T>A
|
XP_005247093.1:p.Ser513=
|
|
NM_018226.6:c.1572T>A
MANE Select
|
NP_060696.4:p.Ser524=
|
|