ENST00000294954.12:c.923T>A
(LHCGR)
MANE Select
|
ENSP00000294954.6:p.Val308Glu
|
|
ENST00000294954.11:c.923T>A
(LHCGR)
|
ENSP00000294954.6:p.Val308Glu
|
|
ENST00000401907.5:c.923T>A
(LHCGR)
|
ENSP00000385406.1:p.Val308Glu
|
|
ENST00000402114.6:c.3441+22568A>T
(STON1-GTF2A1L)
|
ENSP00000385701.1:n.3441+22568A>T
|
|
ENST00000403273.5:c.923T>A
(LHCGR)
|
ENSP00000385847.1:p.Val308Glu
|
|
ENST00000405626.5:c.866+4367T>A
(LHCGR)
|
ENSP00000386033.1:n.866+4367T>A
|
|
ENST00000508440.1:c.276+22568A>T
(GTF2A1L)
|
ENSP00000421474.1:n.276+22568A>T
|
|
ENST00000602369.3:c.*196T>A
|
ENSP00000473498.1:n.*196T>A
|
|
NM_000233.3:c.923T>A
(LHCGR)
|
NP_000224.2:p.Val308Glu
|
|
NM_001198593.1:c.3441+22568A>T
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+22568A>T
|
|
XM_005264309.2:c.-18T>A
(LHCGR)
|
XP_005264366.1:n.-18T>A
|
|
XM_011532828.1:c.848T>A
(LHCGR)
|
XP_011531130.1:p.Val283Glu
|
|
XM_011532829.1:c.662T>A
(LHCGR)
|
XP_011531131.1:p.Val221Glu
|
|
XM_011532830.1:c.606-5399T>A
(LHCGR)
|
XP_011531132.1:n.606-5399T>A
|
|
XM_011532831.1:c.287T>A
(LHCGR)
|
XP_011531133.1:p.Val96Glu
|
|
XM_005264309.3:c.-18T>A
(LHCGR)
|
XP_005264366.1:n.-18T>A
|
|
XM_017004089.1:c.668T>A
(LHCGR)
|
XP_016859578.1:p.Val223Glu
|
|
XM_017004090.1:c.287T>A
(LHCGR)
|
XP_016859579.1:p.Val96Glu
|
|
NM_000233.4:c.923T>A
(LHCGR)
MANE Select
|
NP_000224.2:p.Val308Glu
|
|
NM_001198593.2:c.3441+22568A>T
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+22568A>T
|
|