|
ENST00000294954.12:c.2058A>T
(LHCGR)
MANE Select
|
ENSP00000294954.6:p.Gln686His
|
|
|
ENST00000294954.11:c.2058A>T
(LHCGR)
|
ENSP00000294954.6:p.Gln686His
|
|
|
ENST00000401907.5:c.*370A>T
(LHCGR)
|
ENSP00000385406.1:n.*370A>T
|
|
|
ENST00000402114.6:c.3441+16059T>A
(STON1-GTF2A1L)
|
ENSP00000385701.1:n.3441+16059T>A
|
|
|
ENST00000403273.5:c.*802A>T
(LHCGR)
|
ENSP00000385847.1:n.*802A>T
|
|
|
ENST00000405626.5:c.1977A>T
(LHCGR)
|
ENSP00000386033.1:p.Gln659His
|
|
|
ENST00000508440.1:c.276+16059T>A
(GTF2A1L)
|
ENSP00000421474.1:n.276+16059T>A
|
|
|
ENST00000602369.3:c.*220+6485A>T
|
ENSP00000473498.1:n.*220+6485A>T
|
|
|
NM_000233.3:c.2058A>T
(LHCGR)
|
NP_000224.2:p.Gln686His
|
|
|
NM_001198593.1:c.3441+16059T>A
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16059T>A
|
|
|
XM_005264309.2:c.1101A>T
(LHCGR)
|
XP_005264366.1:p.Gln367His
|
|
|
XM_006712015.2:c.1128A>T
(LHCGR)
|
XP_006712078.1:p.Gln376His
|
|
|
XM_011532828.1:c.1983A>T
(LHCGR)
|
XP_011531130.1:p.Gln661His
|
|
|
XM_011532829.1:c.1797A>T
(LHCGR)
|
XP_011531131.1:p.Gln599His
|
|
|
XM_011532830.1:c.1716A>T
(LHCGR)
|
XP_011531132.1:p.Gln572His
|
|
|
XM_011532831.1:c.1422A>T
(LHCGR)
|
XP_011531133.1:p.Gln474His
|
|
|
XM_011532832.1:c.1128A>T
(LHCGR)
|
XP_011531134.1:p.Gln376His
|
|
|
XM_011532833.1:c.1128A>T
(LHCGR)
|
XP_011531135.1:p.Gln376His
|
|
|
XM_011532834.1:c.1101A>T
(LHCGR)
|
XP_011531136.1:p.Gln367His
|
|
|
XM_005264309.3:c.1101A>T
(LHCGR)
|
XP_005264366.1:p.Gln367His
|
|
|
XM_006712015.3:c.1128A>T
(LHCGR)
|
XP_006712078.1:p.Gln376His
|
|
|
XM_011532834.2:c.1101A>T
(LHCGR)
|
XP_011531136.1:p.Gln367His
|
|
|
XM_017004089.1:c.1803A>T
(LHCGR)
|
XP_016859578.1:p.Gln601His
|
|
|
XM_017004090.1:c.1422A>T
(LHCGR)
|
XP_016859579.1:p.Gln474His
|
|
|
NM_000233.4:c.2058A>T
(LHCGR)
MANE Select
|
NP_000224.2:p.Gln686His
|
|
|
NM_001198593.2:c.3441+16059T>A
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16059T>A
|
|
