ENST00000291547.10:c.523-841G>A
MANE Select
|
ENSP00000291547.4:n.523-841G>A
|
|
ENST00000291547.9:c.523-841G>A
|
ENSP00000291547.4:n.523-841G>A
|
|
ENST00000432907.6:c.172-841G>A
|
ENSP00000402243.2:n.172-841G>A
|
|
ENST00000480179.1:n.582-841G>A
|
|
|
ENST00000560448.5:c.*165-841G>A
|
ENSP00000453486.1:n.*165-841G>A
|
|
NM_001286258.1:c.172-841G>A
|
NP_001273187.1:n.172-841G>A
|
|
NM_004571.4:c.523-841G>A
|
NP_004562.2:n.523-841G>A
|
|
XM_011529604.1:c.523-844G>A
|
XP_011527906.1:n.523-844G>A
|
|
NM_001320694.1:c.523-844G>A
|
NP_001307623.1:n.523-844G>A
|
|
NM_001320694.2:c.523-844G>A
|
NP_001307623.1:n.523-844G>A
|
|
NM_004571.5:c.523-841G>A
MANE Select
|
NP_004562.2:n.523-841G>A
|
|
NM_001286258.2:c.172-841G>A
|
NP_001273187.1:n.172-841G>A
|
|