|
ENST00000294954.12:c.947+19G>T
(LHCGR)
MANE Select
|
ENSP00000294954.6:n.947+19G>T
|
|
|
ENST00000294954.11:c.947+19G>T
(LHCGR)
|
ENSP00000294954.6:n.947+19G>T
|
|
|
ENST00000401907.5:c.947+19G>T
(LHCGR)
|
ENSP00000385406.1:n.947+19G>T
|
|
|
ENST00000402114.6:c.3441+22525C>A
(STON1-GTF2A1L)
|
ENSP00000385701.1:n.3441+22525C>A
|
|
|
ENST00000403273.5:c.947+19G>T
(LHCGR)
|
ENSP00000385847.1:n.947+19G>T
|
|
|
ENST00000405626.5:c.866+4410G>T
(LHCGR)
|
ENSP00000386033.1:n.866+4410G>T
|
|
|
ENST00000508440.1:c.276+22525C>A
(GTF2A1L)
|
ENSP00000421474.1:n.276+22525C>A
|
|
|
ENST00000602369.3:c.*220+19G>T
|
ENSP00000473498.1:n.*220+19G>T
|
|
|
NM_000233.3:c.947+19G>T
(LHCGR)
|
NP_000224.2:n.947+19G>T
|
|
|
NM_001198593.1:c.3441+22525C>A
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+22525C>A
|
|
|
XM_005264309.2:c.-11+36G>T
(LHCGR)
|
XP_005264366.1:n.-11+36G>T
|
|
|
XM_006712015.2:c.-941G>T
(LHCGR)
|
XP_006712078.1:n.-941G>T
|
|
|
XM_011532828.1:c.872+19G>T
(LHCGR)
|
XP_011531130.1:n.872+19G>T
|
|
|
XM_011532829.1:c.686+19G>T
(LHCGR)
|
XP_011531131.1:n.686+19G>T
|
|
|
XM_011532830.1:c.606-5356G>T
(LHCGR)
|
XP_011531132.1:n.606-5356G>T
|
|
|
XM_011532831.1:c.311+19G>T
(LHCGR)
|
XP_011531133.1:n.311+19G>T
|
|
|
XM_011532832.1:c.-508G>T
(LHCGR)
|
XP_011531134.1:n.-508G>T
|
|
|
XM_011532833.1:c.-504G>T
(LHCGR)
|
XP_011531135.1:n.-504G>T
|
|
|
XM_011532834.1:c.-310G>T
(LHCGR)
|
XP_011531136.1:n.-310G>T
|
|
|
XM_005264309.3:c.-11+36G>T
(LHCGR)
|
XP_005264366.1:n.-11+36G>T
|
|
|
XM_006712015.3:c.-941G>T
(LHCGR)
|
XP_006712078.1:n.-941G>T
|
|
|
XM_011532834.2:c.-310G>T
(LHCGR)
|
XP_011531136.1:n.-310G>T
|
|
|
XM_017004089.1:c.692+19G>T
(LHCGR)
|
XP_016859578.1:n.692+19G>T
|
|
|
XM_017004090.1:c.311+19G>T
(LHCGR)
|
XP_016859579.1:n.311+19G>T
|
|
|
NM_000233.4:c.947+19G>T
(LHCGR)
MANE Select
|
NP_000224.2:n.947+19G>T
|
|
|
NM_001198593.2:c.3441+22525C>A
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+22525C>A
|
|
