|
ENST00000294954.12:c.1368C>T
(LHCGR)
MANE Select
|
ENSP00000294954.6:p.Thr456=
|
|
|
ENST00000294954.11:c.1368C>T
(LHCGR)
|
ENSP00000294954.6:p.Thr456=
|
|
|
ENST00000401907.5:c.948-290C>T
(LHCGR)
|
ENSP00000385406.1:n.948-290C>T
|
|
|
ENST00000402114.6:c.3441+16749G>A
(STON1-GTF2A1L)
|
ENSP00000385701.1:n.3441+16749G>A
|
|
|
ENST00000403273.5:c.*112C>T
(LHCGR)
|
ENSP00000385847.1:n.*112C>T
|
|
|
ENST00000405626.5:c.1287C>T
(LHCGR)
|
ENSP00000386033.1:p.Thr429=
|
|
|
ENST00000508440.1:c.276+16749G>A
(GTF2A1L)
|
ENSP00000421474.1:n.276+16749G>A
|
|
|
ENST00000602369.3:c.*220+5795C>T
|
ENSP00000473498.1:n.*220+5795C>T
|
|
|
NM_000233.3:c.1368C>T
(LHCGR)
|
NP_000224.2:p.Thr456=
|
|
|
NM_001198593.1:c.3441+16749G>A
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16749G>A
|
|
|
XM_005264309.2:c.411C>T
(LHCGR)
|
XP_005264366.1:p.Thr137=
|
|
|
XM_006712015.2:c.438C>T
(LHCGR)
|
XP_006712078.1:p.Thr146=
|
|
|
XM_011532828.1:c.1293C>T
(LHCGR)
|
XP_011531130.1:p.Thr431=
|
|
|
XM_011532829.1:c.1107C>T
(LHCGR)
|
XP_011531131.1:p.Thr369=
|
|
|
XM_011532830.1:c.1026C>T
(LHCGR)
|
XP_011531132.1:p.Thr342=
|
|
|
XM_011532831.1:c.732C>T
(LHCGR)
|
XP_011531133.1:p.Thr244=
|
|
|
XM_011532832.1:c.438C>T
(LHCGR)
|
XP_011531134.1:p.Thr146=
|
|
|
XM_011532833.1:c.438C>T
(LHCGR)
|
XP_011531135.1:p.Thr146=
|
|
|
XM_011532834.1:c.411C>T
(LHCGR)
|
XP_011531136.1:p.Thr137=
|
|
|
XM_005264309.3:c.411C>T
(LHCGR)
|
XP_005264366.1:p.Thr137=
|
|
|
XM_006712015.3:c.438C>T
(LHCGR)
|
XP_006712078.1:p.Thr146=
|
|
|
XM_011532834.2:c.411C>T
(LHCGR)
|
XP_011531136.1:p.Thr137=
|
|
|
XM_017004089.1:c.1113C>T
(LHCGR)
|
XP_016859578.1:p.Thr371=
|
|
|
XM_017004090.1:c.732C>T
(LHCGR)
|
XP_016859579.1:p.Thr244=
|
|
|
NM_000233.4:c.1368C>T
(LHCGR)
MANE Select
|
NP_000224.2:p.Thr456=
|
|
|
NM_001198593.2:c.3441+16749G>A
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16749G>A
|
|
