ENST00000270357.10:c.1511-77G>T
MANE Select
|
ENSP00000270357.4:n.1511-77G>T
|
|
ENST00000270357.8:c.818-77G>T
|
ENSP00000270357.3:n.818-77G>T
|
|
ENST00000437406.1:c.110-110G>T
|
ENSP00000403319.1:n.110-110G>T
|
|
ENST00000451363.5:c.152-77G>T
|
ENSP00000414661.1:n.152-77G>T
|
|
ENST00000464550.5:n.347-77G>T
|
|
|
ENST00000471657.1:n.314-77G>T
|
|
|
ENST00000481757.5:n.2368G>T
|
|
|
ENST00000486058.5:n.1624-77G>T
|
|
|
ENST00000493398.5:n.657-77G>T
|
|
|
NM_018226.4:c.1511-77G>T
|
NP_060696.4:n.1511-77G>T
|
|
XM_005247036.3:c.1511-110G>T
|
XP_005247093.1:n.1511-110G>T
|
|
NM_018226.5:c.1511-77G>T
|
NP_060696.4:n.1511-77G>T
|
|
XM_005247036.4:c.1511-110G>T
|
XP_005247093.1:n.1511-110G>T
|
|
NM_018226.6:c.1511-77G>T
MANE Select
|
NP_060696.4:n.1511-77G>T
|
|