ENST00000251535.11:c.337+12G>T
(ALOX12)
MANE Select
|
ENSP00000251535.6:n.337+12G>T
|
|
ENST00000251535.10:c.337+12G>T
(ALOX12)
|
ENSP00000251535.6:n.337+12G>T
|
|
ENST00000480801.1:c.46+12G>T
(ALOX12)
|
ENSP00000467033.1:n.46+12G>T
|
|
NM_000697.2:c.337+12G>T
(ALOX12)
|
NP_000688.2:n.337+12G>T
|
|
NR_040089.1:n.234-11499C>A
(ALOX12-AS1)
|
|
|
XM_011523780.1:c.694+12G>T
(ALOX12)
|
XP_011522082.1:n.694+12G>T
|
|
XM_011523780.2:c.694+12G>T
(ALOX12)
|
XP_011522082.1:n.694+12G>T
|
|
NM_000697.3:c.337+12G>T
(ALOX12)
MANE Select
|
NP_000688.2:n.337+12G>T
|
|