ENST00000270357.10:c.1551G>T
MANE Select
|
ENSP00000270357.4:p.Pro517=
|
|
ENST00000270357.8:c.858G>T
|
ENSP00000270357.3:p.Pro286=
|
|
ENST00000437406.1:c.117G>T
|
ENSP00000403319.1:p.Pro39=
|
|
ENST00000451363.5:c.192G>T
|
ENSP00000414661.1:p.Pro64=
|
|
ENST00000464550.5:n.387G>T
|
|
|
ENST00000471657.1:n.354G>T
|
|
|
ENST00000481757.5:n.2485G>T
|
|
|
ENST00000486058.5:n.1664G>T
|
|
|
ENST00000493398.5:n.697G>T
|
|
|
NM_018226.4:c.1551G>T
|
NP_060696.4:p.Pro517=
|
|
XM_005247036.3:c.1518G>T
|
XP_005247093.1:p.Pro506=
|
|
NM_018226.5:c.1551G>T
|
NP_060696.4:p.Pro517=
|
|
XM_005247036.4:c.1518G>T
|
XP_005247093.1:p.Pro506=
|
|
NM_018226.6:c.1551G>T
MANE Select
|
NP_060696.4:p.Pro517=
|
|