ENST00000294954.12:c.1639A>T
(LHCGR)
MANE Select
|
ENSP00000294954.6:p.Ile547Phe
|
|
ENST00000294954.11:c.1639A>T
(LHCGR)
|
ENSP00000294954.6:p.Ile547Phe
|
|
ENST00000401907.5:c.948-19A>T
(LHCGR)
|
ENSP00000385406.1:n.948-19A>T
|
|
ENST00000402114.6:c.3441+16478T>A
(STON1-GTF2A1L)
|
ENSP00000385701.1:n.3441+16478T>A
|
|
ENST00000403273.5:c.*383A>T
(LHCGR)
|
ENSP00000385847.1:n.*383A>T
|
|
ENST00000405626.5:c.1558A>T
(LHCGR)
|
ENSP00000386033.1:p.Ile520Phe
|
|
ENST00000508440.1:c.276+16478T>A
(GTF2A1L)
|
ENSP00000421474.1:n.276+16478T>A
|
|
ENST00000602369.3:c.*220+6066A>T
|
ENSP00000473498.1:n.*220+6066A>T
|
|
NM_000233.3:c.1639A>T
(LHCGR)
|
NP_000224.2:p.Ile547Phe
|
|
NM_001198593.1:c.3441+16478T>A
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16478T>A
|
|
XM_005264309.2:c.682A>T
(LHCGR)
|
XP_005264366.1:p.Ile228Phe
|
|
XM_006712015.2:c.709A>T
(LHCGR)
|
XP_006712078.1:p.Ile237Phe
|
|
XM_011532828.1:c.1564A>T
(LHCGR)
|
XP_011531130.1:p.Ile522Phe
|
|
XM_011532829.1:c.1378A>T
(LHCGR)
|
XP_011531131.1:p.Ile460Phe
|
|
XM_011532830.1:c.1297A>T
(LHCGR)
|
XP_011531132.1:p.Ile433Phe
|
|
XM_011532831.1:c.1003A>T
(LHCGR)
|
XP_011531133.1:p.Ile335Phe
|
|
XM_011532832.1:c.709A>T
(LHCGR)
|
XP_011531134.1:p.Ile237Phe
|
|
XM_011532833.1:c.709A>T
(LHCGR)
|
XP_011531135.1:p.Ile237Phe
|
|
XM_011532834.1:c.682A>T
(LHCGR)
|
XP_011531136.1:p.Ile228Phe
|
|
XM_005264309.3:c.682A>T
(LHCGR)
|
XP_005264366.1:p.Ile228Phe
|
|
XM_006712015.3:c.709A>T
(LHCGR)
|
XP_006712078.1:p.Ile237Phe
|
|
XM_011532834.2:c.682A>T
(LHCGR)
|
XP_011531136.1:p.Ile228Phe
|
|
XM_017004089.1:c.1384A>T
(LHCGR)
|
XP_016859578.1:p.Ile462Phe
|
|
XM_017004090.1:c.1003A>T
(LHCGR)
|
XP_016859579.1:p.Ile335Phe
|
|
NM_000233.4:c.1639A>T
(LHCGR)
MANE Select
|
NP_000224.2:p.Ile547Phe
|
|
NM_001198593.2:c.3441+16478T>A
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16478T>A
|
|