|
ENST00000294954.12:c.1360G>T
(LHCGR)
MANE Select
|
ENSP00000294954.6:p.Val454Phe
|
|
|
ENST00000294954.11:c.1360G>T
(LHCGR)
|
ENSP00000294954.6:p.Val454Phe
|
|
|
ENST00000401907.5:c.948-298G>T
(LHCGR)
|
ENSP00000385406.1:n.948-298G>T
|
|
|
ENST00000402114.6:c.3441+16757C>A
(STON1-GTF2A1L)
|
ENSP00000385701.1:n.3441+16757C>A
|
|
|
ENST00000403273.5:c.*104G>T
(LHCGR)
|
ENSP00000385847.1:n.*104G>T
|
|
|
ENST00000405626.5:c.1279G>T
(LHCGR)
|
ENSP00000386033.1:p.Val427Phe
|
|
|
ENST00000508440.1:c.276+16757C>A
(GTF2A1L)
|
ENSP00000421474.1:n.276+16757C>A
|
|
|
ENST00000602369.3:c.*220+5787G>T
|
ENSP00000473498.1:n.*220+5787G>T
|
|
|
NM_000233.3:c.1360G>T
(LHCGR)
|
NP_000224.2:p.Val454Phe
|
|
|
NM_001198593.1:c.3441+16757C>A
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16757C>A
|
|
|
XM_005264309.2:c.403G>T
(LHCGR)
|
XP_005264366.1:p.Val135Phe
|
|
|
XM_006712015.2:c.430G>T
(LHCGR)
|
XP_006712078.1:p.Val144Phe
|
|
|
XM_011532828.1:c.1285G>T
(LHCGR)
|
XP_011531130.1:p.Val429Phe
|
|
|
XM_011532829.1:c.1099G>T
(LHCGR)
|
XP_011531131.1:p.Val367Phe
|
|
|
XM_011532830.1:c.1018G>T
(LHCGR)
|
XP_011531132.1:p.Val340Phe
|
|
|
XM_011532831.1:c.724G>T
(LHCGR)
|
XP_011531133.1:p.Val242Phe
|
|
|
XM_011532832.1:c.430G>T
(LHCGR)
|
XP_011531134.1:p.Val144Phe
|
|
|
XM_011532833.1:c.430G>T
(LHCGR)
|
XP_011531135.1:p.Val144Phe
|
|
|
XM_011532834.1:c.403G>T
(LHCGR)
|
XP_011531136.1:p.Val135Phe
|
|
|
XM_005264309.3:c.403G>T
(LHCGR)
|
XP_005264366.1:p.Val135Phe
|
|
|
XM_006712015.3:c.430G>T
(LHCGR)
|
XP_006712078.1:p.Val144Phe
|
|
|
XM_011532834.2:c.403G>T
(LHCGR)
|
XP_011531136.1:p.Val135Phe
|
|
|
XM_017004089.1:c.1105G>T
(LHCGR)
|
XP_016859578.1:p.Val369Phe
|
|
|
XM_017004090.1:c.724G>T
(LHCGR)
|
XP_016859579.1:p.Val242Phe
|
|
|
NM_000233.4:c.1360G>T
(LHCGR)
MANE Select
|
NP_000224.2:p.Val454Phe
|
|
|
NM_001198593.2:c.3441+16757C>A
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16757C>A
|
|
