|
ENST00000294954.12:c.1906C>G
(LHCGR)
MANE Select
|
ENSP00000294954.6:p.Leu636Val
|
|
|
ENST00000294954.11:c.1906C>G
(LHCGR)
|
ENSP00000294954.6:p.Leu636Val
|
|
|
ENST00000401907.5:c.*218C>G
(LHCGR)
|
ENSP00000385406.1:n.*218C>G
|
|
|
ENST00000402114.6:c.3441+16211G>C
(STON1-GTF2A1L)
|
ENSP00000385701.1:n.3441+16211G>C
|
|
|
ENST00000403273.5:c.*650C>G
(LHCGR)
|
ENSP00000385847.1:n.*650C>G
|
|
|
ENST00000405626.5:c.1825C>G
(LHCGR)
|
ENSP00000386033.1:p.Leu609Val
|
|
|
ENST00000508440.1:c.276+16211G>C
(GTF2A1L)
|
ENSP00000421474.1:n.276+16211G>C
|
|
|
ENST00000602369.3:c.*220+6333C>G
|
ENSP00000473498.1:n.*220+6333C>G
|
|
|
NM_000233.3:c.1906C>G
(LHCGR)
|
NP_000224.2:p.Leu636Val
|
|
|
NM_001198593.1:c.3441+16211G>C
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16211G>C
|
|
|
XM_005264309.2:c.949C>G
(LHCGR)
|
XP_005264366.1:p.Leu317Val
|
|
|
XM_006712015.2:c.976C>G
(LHCGR)
|
XP_006712078.1:p.Leu326Val
|
|
|
XM_011532828.1:c.1831C>G
(LHCGR)
|
XP_011531130.1:p.Leu611Val
|
|
|
XM_011532829.1:c.1645C>G
(LHCGR)
|
XP_011531131.1:p.Leu549Val
|
|
|
XM_011532830.1:c.1564C>G
(LHCGR)
|
XP_011531132.1:p.Leu522Val
|
|
|
XM_011532831.1:c.1270C>G
(LHCGR)
|
XP_011531133.1:p.Leu424Val
|
|
|
XM_011532832.1:c.976C>G
(LHCGR)
|
XP_011531134.1:p.Leu326Val
|
|
|
XM_011532833.1:c.976C>G
(LHCGR)
|
XP_011531135.1:p.Leu326Val
|
|
|
XM_011532834.1:c.949C>G
(LHCGR)
|
XP_011531136.1:p.Leu317Val
|
|
|
XM_005264309.3:c.949C>G
(LHCGR)
|
XP_005264366.1:p.Leu317Val
|
|
|
XM_006712015.3:c.976C>G
(LHCGR)
|
XP_006712078.1:p.Leu326Val
|
|
|
XM_011532834.2:c.949C>G
(LHCGR)
|
XP_011531136.1:p.Leu317Val
|
|
|
XM_017004089.1:c.1651C>G
(LHCGR)
|
XP_016859578.1:p.Leu551Val
|
|
|
XM_017004090.1:c.1270C>G
(LHCGR)
|
XP_016859579.1:p.Leu424Val
|
|
|
NM_000233.4:c.1906C>G
(LHCGR)
MANE Select
|
NP_000224.2:p.Leu636Val
|
|
|
NM_001198593.2:c.3441+16211G>C
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16211G>C
|
|
