ENST00000294954.12:c.2100A>G
(LHCGR)
MANE Select
|
ENSP00000294954.6:p.Ter700=
|
|
ENST00000294954.11:c.2100A>G
(LHCGR)
|
ENSP00000294954.6:p.Ter700=
|
|
ENST00000401907.5:c.*412A>G
(LHCGR)
|
ENSP00000385406.1:n.*412A>G
|
|
ENST00000402114.6:c.3441+16017T>C
(STON1-GTF2A1L)
|
ENSP00000385701.1:n.3441+16017T>C
|
|
ENST00000403273.5:c.*844A>G
(LHCGR)
|
ENSP00000385847.1:n.*844A>G
|
|
ENST00000405626.5:c.2019A>G
(LHCGR)
|
ENSP00000386033.1:p.Ter673=
|
|
ENST00000508440.1:c.276+16017T>C
(GTF2A1L)
|
ENSP00000421474.1:n.276+16017T>C
|
|
ENST00000602369.3:c.*220+6527A>G
|
ENSP00000473498.1:n.*220+6527A>G
|
|
NM_000233.3:c.2100A>G
(LHCGR)
|
NP_000224.2:p.Ter700=
|
|
NM_001198593.1:c.3441+16017T>C
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16017T>C
|
|
XM_005264309.2:c.1143A>G
(LHCGR)
|
XP_005264366.1:p.Ter381=
|
|
XM_006712015.2:c.1170A>G
(LHCGR)
|
XP_006712078.1:p.Ter390=
|
|
XM_011532828.1:c.2025A>G
(LHCGR)
|
XP_011531130.1:p.Ter675=
|
|
XM_011532829.1:c.1839A>G
(LHCGR)
|
XP_011531131.1:p.Ter613=
|
|
XM_011532830.1:c.1758A>G
(LHCGR)
|
XP_011531132.1:p.Ter586=
|
|
XM_011532831.1:c.1464A>G
(LHCGR)
|
XP_011531133.1:p.Ter488=
|
|
XM_011532832.1:c.1170A>G
(LHCGR)
|
XP_011531134.1:p.Ter390=
|
|
XM_011532833.1:c.1170A>G
(LHCGR)
|
XP_011531135.1:p.Ter390=
|
|
XM_011532834.1:c.1143A>G
(LHCGR)
|
XP_011531136.1:p.Ter381=
|
|
XM_005264309.3:c.1143A>G
(LHCGR)
|
XP_005264366.1:p.Ter381=
|
|
XM_006712015.3:c.1170A>G
(LHCGR)
|
XP_006712078.1:p.Ter390=
|
|
XM_011532834.2:c.1143A>G
(LHCGR)
|
XP_011531136.1:p.Ter381=
|
|
XM_017004089.1:c.1845A>G
(LHCGR)
|
XP_016859578.1:p.Ter615=
|
|
XM_017004090.1:c.1464A>G
(LHCGR)
|
XP_016859579.1:p.Ter488=
|
|
NM_000233.4:c.2100A>G
(LHCGR)
MANE Select
|
NP_000224.2:p.Ter700=
|
|
NM_001198593.2:c.3441+16017T>C
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16017T>C
|
|