ENST00000609713.2:c.947-29486C>T
MANE Select
|
ENSP00000477437.1:n.947-29486C>T
|
|
ENST00000645093.1:c.947-29486C>T
|
ENSP00000493772.1:n.947-29486C>T
|
|
ENST00000609713.1:c.947-29486C>T
|
ENSP00000477437.1:n.947-29486C>T
|
|
NM_002240.3:c.947-29486C>T
|
NP_002231.1:n.947-29486C>T
|
|
NM_002240.4:c.947-29486C>T
|
NP_002231.1:n.947-29486C>T
|
|
XM_011529558.1:c.947-29486C>T
|
XP_011527860.1:n.947-29486C>T
|
|
XM_011529559.1:c.947-29486C>T
|
XP_011527861.1:n.947-29486C>T
|
|
NM_002240.5:c.947-29486C>T
MANE Select
|
NP_002231.1:n.947-29486C>T
|
|