|
ENST00000294954.12:c.2073A>T
(LHCGR)
MANE Select
|
ENSP00000294954.6:p.Leu691=
|
|
|
ENST00000294954.11:c.2073A>T
(LHCGR)
|
ENSP00000294954.6:p.Leu691=
|
|
|
ENST00000401907.5:c.*385A>T
(LHCGR)
|
ENSP00000385406.1:n.*385A>T
|
|
|
ENST00000402114.6:c.3441+16044T>A
(STON1-GTF2A1L)
|
ENSP00000385701.1:n.3441+16044T>A
|
|
|
ENST00000403273.5:c.*817A>T
(LHCGR)
|
ENSP00000385847.1:n.*817A>T
|
|
|
ENST00000405626.5:c.1992A>T
(LHCGR)
|
ENSP00000386033.1:p.Leu664=
|
|
|
ENST00000508440.1:c.276+16044T>A
(GTF2A1L)
|
ENSP00000421474.1:n.276+16044T>A
|
|
|
ENST00000602369.3:c.*220+6500A>T
|
ENSP00000473498.1:n.*220+6500A>T
|
|
|
NM_000233.3:c.2073A>T
(LHCGR)
|
NP_000224.2:p.Leu691=
|
|
|
NM_001198593.1:c.3441+16044T>A
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16044T>A
|
|
|
XM_005264309.2:c.1116A>T
(LHCGR)
|
XP_005264366.1:p.Leu372=
|
|
|
XM_006712015.2:c.1143A>T
(LHCGR)
|
XP_006712078.1:p.Leu381=
|
|
|
XM_011532828.1:c.1998A>T
(LHCGR)
|
XP_011531130.1:p.Leu666=
|
|
|
XM_011532829.1:c.1812A>T
(LHCGR)
|
XP_011531131.1:p.Leu604=
|
|
|
XM_011532830.1:c.1731A>T
(LHCGR)
|
XP_011531132.1:p.Leu577=
|
|
|
XM_011532831.1:c.1437A>T
(LHCGR)
|
XP_011531133.1:p.Leu479=
|
|
|
XM_011532832.1:c.1143A>T
(LHCGR)
|
XP_011531134.1:p.Leu381=
|
|
|
XM_011532833.1:c.1143A>T
(LHCGR)
|
XP_011531135.1:p.Leu381=
|
|
|
XM_011532834.1:c.1116A>T
(LHCGR)
|
XP_011531136.1:p.Leu372=
|
|
|
XM_005264309.3:c.1116A>T
(LHCGR)
|
XP_005264366.1:p.Leu372=
|
|
|
XM_006712015.3:c.1143A>T
(LHCGR)
|
XP_006712078.1:p.Leu381=
|
|
|
XM_011532834.2:c.1116A>T
(LHCGR)
|
XP_011531136.1:p.Leu372=
|
|
|
XM_017004089.1:c.1818A>T
(LHCGR)
|
XP_016859578.1:p.Leu606=
|
|
|
XM_017004090.1:c.1437A>T
(LHCGR)
|
XP_016859579.1:p.Leu479=
|
|
|
NM_000233.4:c.2073A>T
(LHCGR)
MANE Select
|
NP_000224.2:p.Leu691=
|
|
|
NM_001198593.2:c.3441+16044T>A
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16044T>A
|
|
