ENST00000270357.10:c.1590C>G
MANE Select
|
ENSP00000270357.4:p.Thr530=
|
|
ENST00000270357.8:c.897C>G
|
ENSP00000270357.3:p.Thr299=
|
|
ENST00000437406.1:c.156C>G
|
ENSP00000403319.1:p.Thr52=
|
|
ENST00000451363.5:c.231C>G
|
ENSP00000414661.1:p.Thr77=
|
|
ENST00000464550.5:n.426C>G
|
|
|
ENST00000471657.1:n.393C>G
|
|
|
ENST00000481757.5:n.2524C>G
|
|
|
ENST00000486058.5:n.1703C>G
|
|
|
ENST00000493398.5:n.736C>G
|
|
|
NM_018226.4:c.1590C>G
|
NP_060696.4:p.Thr530=
|
|
XM_005247036.3:c.1557C>G
|
XP_005247093.1:p.Thr519=
|
|
NM_018226.5:c.1590C>G
|
NP_060696.4:p.Thr530=
|
|
XM_005247036.4:c.1557C>G
|
XP_005247093.1:p.Thr519=
|
|
NM_018226.6:c.1590C>G
MANE Select
|
NP_060696.4:p.Thr530=
|
|