ENST00000294954.12:c.1988G>A
(LHCGR)
MANE Select
|
ENSP00000294954.6:p.Cys663Tyr
|
|
ENST00000294954.11:c.1988G>A
(LHCGR)
|
ENSP00000294954.6:p.Cys663Tyr
|
|
ENST00000401907.5:c.*300G>A
(LHCGR)
|
ENSP00000385406.1:n.*300G>A
|
|
ENST00000402114.6:c.3441+16129C>T
(STON1-GTF2A1L)
|
ENSP00000385701.1:n.3441+16129C>T
|
|
ENST00000403273.5:c.*732G>A
(LHCGR)
|
ENSP00000385847.1:n.*732G>A
|
|
ENST00000405626.5:c.1907G>A
(LHCGR)
|
ENSP00000386033.1:p.Cys636Tyr
|
|
ENST00000508440.1:c.276+16129C>T
(GTF2A1L)
|
ENSP00000421474.1:n.276+16129C>T
|
|
ENST00000602369.3:c.*220+6415G>A
|
ENSP00000473498.1:n.*220+6415G>A
|
|
NM_000233.3:c.1988G>A
(LHCGR)
|
NP_000224.2:p.Cys663Tyr
|
|
NM_001198593.1:c.3441+16129C>T
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16129C>T
|
|
XM_005264309.2:c.1031G>A
(LHCGR)
|
XP_005264366.1:p.Cys344Tyr
|
|
XM_006712015.2:c.1058G>A
(LHCGR)
|
XP_006712078.1:p.Cys353Tyr
|
|
XM_011532828.1:c.1913G>A
(LHCGR)
|
XP_011531130.1:p.Cys638Tyr
|
|
XM_011532829.1:c.1727G>A
(LHCGR)
|
XP_011531131.1:p.Cys576Tyr
|
|
XM_011532830.1:c.1646G>A
(LHCGR)
|
XP_011531132.1:p.Cys549Tyr
|
|
XM_011532831.1:c.1352G>A
(LHCGR)
|
XP_011531133.1:p.Cys451Tyr
|
|
XM_011532832.1:c.1058G>A
(LHCGR)
|
XP_011531134.1:p.Cys353Tyr
|
|
XM_011532833.1:c.1058G>A
(LHCGR)
|
XP_011531135.1:p.Cys353Tyr
|
|
XM_011532834.1:c.1031G>A
(LHCGR)
|
XP_011531136.1:p.Cys344Tyr
|
|
XM_005264309.3:c.1031G>A
(LHCGR)
|
XP_005264366.1:p.Cys344Tyr
|
|
XM_006712015.3:c.1058G>A
(LHCGR)
|
XP_006712078.1:p.Cys353Tyr
|
|
XM_011532834.2:c.1031G>A
(LHCGR)
|
XP_011531136.1:p.Cys344Tyr
|
|
XM_017004089.1:c.1733G>A
(LHCGR)
|
XP_016859578.1:p.Cys578Tyr
|
|
XM_017004090.1:c.1352G>A
(LHCGR)
|
XP_016859579.1:p.Cys451Tyr
|
|
NM_000233.4:c.1988G>A
(LHCGR)
MANE Select
|
NP_000224.2:p.Cys663Tyr
|
|
NM_001198593.2:c.3441+16129C>T
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16129C>T
|
|