ENST00000294954.12:c.1802T>A
(LHCGR)
MANE Select
|
ENSP00000294954.6:p.Val601Glu
|
|
ENST00000294954.11:c.1802T>A
(LHCGR)
|
ENSP00000294954.6:p.Val601Glu
|
|
ENST00000401907.5:c.*114T>A
(LHCGR)
|
ENSP00000385406.1:n.*114T>A
|
|
ENST00000402114.6:c.3441+16315A>T
(STON1-GTF2A1L)
|
ENSP00000385701.1:n.3441+16315A>T
|
|
ENST00000403273.5:c.*546T>A
(LHCGR)
|
ENSP00000385847.1:n.*546T>A
|
|
ENST00000405626.5:c.1721T>A
(LHCGR)
|
ENSP00000386033.1:p.Val574Glu
|
|
ENST00000508440.1:c.276+16315A>T
(GTF2A1L)
|
ENSP00000421474.1:n.276+16315A>T
|
|
ENST00000602369.3:c.*220+6229T>A
|
ENSP00000473498.1:n.*220+6229T>A
|
|
NM_000233.3:c.1802T>A
(LHCGR)
|
NP_000224.2:p.Val601Glu
|
|
NM_001198593.1:c.3441+16315A>T
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16315A>T
|
|
XM_005264309.2:c.845T>A
(LHCGR)
|
XP_005264366.1:p.Val282Glu
|
|
XM_006712015.2:c.872T>A
(LHCGR)
|
XP_006712078.1:p.Val291Glu
|
|
XM_011532828.1:c.1727T>A
(LHCGR)
|
XP_011531130.1:p.Val576Glu
|
|
XM_011532829.1:c.1541T>A
(LHCGR)
|
XP_011531131.1:p.Val514Glu
|
|
XM_011532830.1:c.1460T>A
(LHCGR)
|
XP_011531132.1:p.Val487Glu
|
|
XM_011532831.1:c.1166T>A
(LHCGR)
|
XP_011531133.1:p.Val389Glu
|
|
XM_011532832.1:c.872T>A
(LHCGR)
|
XP_011531134.1:p.Val291Glu
|
|
XM_011532833.1:c.872T>A
(LHCGR)
|
XP_011531135.1:p.Val291Glu
|
|
XM_011532834.1:c.845T>A
(LHCGR)
|
XP_011531136.1:p.Val282Glu
|
|
XM_005264309.3:c.845T>A
(LHCGR)
|
XP_005264366.1:p.Val282Glu
|
|
XM_006712015.3:c.872T>A
(LHCGR)
|
XP_006712078.1:p.Val291Glu
|
|
XM_011532834.2:c.845T>A
(LHCGR)
|
XP_011531136.1:p.Val282Glu
|
|
XM_017004089.1:c.1547T>A
(LHCGR)
|
XP_016859578.1:p.Val516Glu
|
|
XM_017004090.1:c.1166T>A
(LHCGR)
|
XP_016859579.1:p.Val389Glu
|
|
NM_000233.4:c.1802T>A
(LHCGR)
MANE Select
|
NP_000224.2:p.Val601Glu
|
|
NM_001198593.2:c.3441+16315A>T
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16315A>T
|
|