ENST00000294954.12:c.866+8G>A
(LHCGR)
MANE Select
|
ENSP00000294954.6:n.866+8G>A
|
|
ENST00000294954.11:c.866+8G>A
(LHCGR)
|
ENSP00000294954.6:n.866+8G>A
|
|
ENST00000401907.5:c.866+8G>A
(LHCGR)
|
ENSP00000385406.1:n.866+8G>A
|
|
ENST00000402114.6:c.3441+26927C>T
(STON1-GTF2A1L)
|
ENSP00000385701.1:n.3441+26927C>T
|
|
ENST00000403273.5:c.866+8G>A
(LHCGR)
|
ENSP00000385847.1:n.866+8G>A
|
|
ENST00000405626.5:c.866+8G>A
(LHCGR)
|
ENSP00000386033.1:n.866+8G>A
|
|
ENST00000508440.1:c.276+26927C>T
(GTF2A1L)
|
ENSP00000421474.1:n.276+26927C>T
|
|
ENST00000602369.3:c.*139+8G>A
|
ENSP00000473498.1:n.*139+8G>A
|
|
NM_000233.3:c.866+8G>A
(LHCGR)
|
NP_000224.2:n.866+8G>A
|
|
NM_001198593.1:c.3441+26927C>T
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+26927C>T
|
|
XM_011532828.1:c.791+8G>A
(LHCGR)
|
XP_011531130.1:n.791+8G>A
|
|
XM_011532829.1:c.606-4303G>A
(LHCGR)
|
XP_011531131.1:n.606-4303G>A
|
|
XM_011532830.1:c.606-9758G>A
(LHCGR)
|
XP_011531132.1:n.606-9758G>A
|
|
XM_011532831.1:c.230+8G>A
(LHCGR)
|
XP_011531133.1:n.230+8G>A
|
|
XM_017004089.1:c.612-4303G>A
(LHCGR)
|
XP_016859578.1:n.612-4303G>A
|
|
XM_017004090.1:c.230+8G>A
(LHCGR)
|
XP_016859579.1:n.230+8G>A
|
|
NM_000233.4:c.866+8G>A
(LHCGR)
MANE Select
|
NP_000224.2:n.866+8G>A
|
|
NM_001198593.2:c.3441+26927C>T
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+26927C>T
|
|