ENST00000172229.8:c.569-1659_569-1658insA
(NGFR)
MANE Select
|
ENSP00000172229.3:n.569-1659_569-1658insA
|
|
ENST00000172229.7:c.569-1659_569-1658insA
(NGFR)
|
ENSP00000172229.3:n.569-1659_569-1658insA
|
|
ENST00000504201.1:c.287-1659_287-1658insA
(NGFR)
|
ENSP00000421731.1:n.287-1659_287-1658insA
|
|
NM_002507.3:c.569-1659_569-1658insA
(NGFR)
|
NP_002498.1:n.569-1659_569-1658insA
|
|
NR_103773.1:n.377+2229_377+2230insT
(NGFR-AS1)
|
|
|
NM_002507.4:c.569-1659_569-1658insA
(NGFR)
MANE Select
|
NP_002498.1:n.569-1659_569-1658insA
|
|