ENST00000294954.12:c.1804A>G
(LHCGR)
MANE Select
|
ENSP00000294954.6:p.Thr602Ala
|
|
ENST00000294954.11:c.1804A>G
(LHCGR)
|
ENSP00000294954.6:p.Thr602Ala
|
|
ENST00000401907.5:c.*116A>G
(LHCGR)
|
ENSP00000385406.1:n.*116A>G
|
|
ENST00000402114.6:c.3441+16313T>C
(STON1-GTF2A1L)
|
ENSP00000385701.1:n.3441+16313T>C
|
|
ENST00000403273.5:c.*548A>G
(LHCGR)
|
ENSP00000385847.1:n.*548A>G
|
|
ENST00000405626.5:c.1723A>G
(LHCGR)
|
ENSP00000386033.1:p.Thr575Ala
|
|
ENST00000508440.1:c.276+16313T>C
(GTF2A1L)
|
ENSP00000421474.1:n.276+16313T>C
|
|
ENST00000602369.3:c.*220+6231A>G
|
ENSP00000473498.1:n.*220+6231A>G
|
|
NM_000233.3:c.1804A>G
(LHCGR)
|
NP_000224.2:p.Thr602Ala
|
|
NM_001198593.1:c.3441+16313T>C
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16313T>C
|
|
XM_005264309.2:c.847A>G
(LHCGR)
|
XP_005264366.1:p.Thr283Ala
|
|
XM_006712015.2:c.874A>G
(LHCGR)
|
XP_006712078.1:p.Thr292Ala
|
|
XM_011532828.1:c.1729A>G
(LHCGR)
|
XP_011531130.1:p.Thr577Ala
|
|
XM_011532829.1:c.1543A>G
(LHCGR)
|
XP_011531131.1:p.Thr515Ala
|
|
XM_011532830.1:c.1462A>G
(LHCGR)
|
XP_011531132.1:p.Thr488Ala
|
|
XM_011532831.1:c.1168A>G
(LHCGR)
|
XP_011531133.1:p.Thr390Ala
|
|
XM_011532832.1:c.874A>G
(LHCGR)
|
XP_011531134.1:p.Thr292Ala
|
|
XM_011532833.1:c.874A>G
(LHCGR)
|
XP_011531135.1:p.Thr292Ala
|
|
XM_011532834.1:c.847A>G
(LHCGR)
|
XP_011531136.1:p.Thr283Ala
|
|
XM_005264309.3:c.847A>G
(LHCGR)
|
XP_005264366.1:p.Thr283Ala
|
|
XM_006712015.3:c.874A>G
(LHCGR)
|
XP_006712078.1:p.Thr292Ala
|
|
XM_011532834.2:c.847A>G
(LHCGR)
|
XP_011531136.1:p.Thr283Ala
|
|
XM_017004089.1:c.1549A>G
(LHCGR)
|
XP_016859578.1:p.Thr517Ala
|
|
XM_017004090.1:c.1168A>G
(LHCGR)
|
XP_016859579.1:p.Thr390Ala
|
|
NM_000233.4:c.1804A>G
(LHCGR)
MANE Select
|
NP_000224.2:p.Thr602Ala
|
|
NM_001198593.2:c.3441+16313T>C
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16313T>C
|
|