ENST00000270357.10:c.1599G>A
MANE Select
|
ENSP00000270357.4:p.Val533=
|
|
ENST00000270357.8:c.906G>A
|
ENSP00000270357.3:p.Val302=
|
|
ENST00000437406.1:c.165G>A
|
ENSP00000403319.1:p.Val55=
|
|
ENST00000451363.5:c.240G>A
|
ENSP00000414661.1:p.Val80=
|
|
ENST00000464550.5:n.435G>A
|
|
|
ENST00000471657.1:n.402G>A
|
|
|
ENST00000481757.5:n.2533G>A
|
|
|
ENST00000486058.5:n.1712G>A
|
|
|
ENST00000493398.5:n.745G>A
|
|
|
NM_018226.4:c.1599G>A
|
NP_060696.4:p.Val533=
|
|
XM_005247036.3:c.1566G>A
|
XP_005247093.1:p.Val522=
|
|
NM_018226.5:c.1599G>A
|
NP_060696.4:p.Val533=
|
|
XM_005247036.4:c.1566G>A
|
XP_005247093.1:p.Val522=
|
|
NM_018226.6:c.1599G>A
MANE Select
|
NP_060696.4:p.Val533=
|
|