ENST00000270357.10:c.1622C>G
MANE Select
|
ENSP00000270357.4:p.Thr541Ser
|
|
ENST00000270357.8:c.929C>G
|
ENSP00000270357.3:p.Thr310Ser
|
|
ENST00000437406.1:c.188C>G
|
ENSP00000403319.1:p.Thr63Ser
|
|
ENST00000451363.5:c.263C>G
|
ENSP00000414661.1:p.Thr88Ser
|
|
ENST00000464550.5:n.458C>G
|
|
|
ENST00000471657.1:n.425C>G
|
|
|
ENST00000481757.5:n.2556C>G
|
|
|
ENST00000486058.5:n.1735C>G
|
|
|
ENST00000493398.5:n.768C>G
|
|
|
NM_018226.4:c.1622C>G
|
NP_060696.4:p.Thr541Ser
|
|
XM_005247036.3:c.1589C>G
|
XP_005247093.1:p.Thr530Ser
|
|
NM_018226.5:c.1622C>G
|
NP_060696.4:p.Thr541Ser
|
|
XM_005247036.4:c.1589C>G
|
XP_005247093.1:p.Thr530Ser
|
|
NM_018226.6:c.1622C>G
MANE Select
|
NP_060696.4:p.Thr541Ser
|
|