|
ENST00000294954.12:c.965C>T
(LHCGR)
MANE Select
|
ENSP00000294954.6:p.Ala322Val
|
|
|
ENST00000294954.11:c.965C>T
(LHCGR)
|
ENSP00000294954.6:p.Ala322Val
|
|
|
ENST00000401907.5:c.948-693C>T
(LHCGR)
|
ENSP00000385406.1:n.948-693C>T
|
|
|
ENST00000402114.6:c.3441+17152G>A
(STON1-GTF2A1L)
|
ENSP00000385701.1:n.3441+17152G>A
|
|
|
ENST00000403273.5:c.948-249C>T
(LHCGR)
|
ENSP00000385847.1:n.948-249C>T
|
|
|
ENST00000405626.5:c.884C>T
(LHCGR)
|
ENSP00000386033.1:p.Ala295Val
|
|
|
ENST00000508440.1:c.276+17152G>A
(GTF2A1L)
|
ENSP00000421474.1:n.276+17152G>A
|
|
|
ENST00000602369.3:c.*220+5392C>T
|
ENSP00000473498.1:n.*220+5392C>T
|
|
|
NM_000233.3:c.965C>T
(LHCGR)
|
NP_000224.2:p.Ala322Val
|
|
|
NM_001198593.1:c.3441+17152G>A
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+17152G>A
|
|
|
XM_005264309.2:c.8C>T
(LHCGR)
|
XP_005264366.1:p.Ala3Val
|
|
|
XM_006712015.2:c.35C>T
(LHCGR)
|
XP_006712078.1:p.Ala12Val
|
|
|
XM_011532828.1:c.890C>T
(LHCGR)
|
XP_011531130.1:p.Ala297Val
|
|
|
XM_011532829.1:c.704C>T
(LHCGR)
|
XP_011531131.1:p.Ala235Val
|
|
|
XM_011532830.1:c.623C>T
(LHCGR)
|
XP_011531132.1:p.Ala208Val
|
|
|
XM_011532831.1:c.329C>T
(LHCGR)
|
XP_011531133.1:p.Ala110Val
|
|
|
XM_011532832.1:c.35C>T
(LHCGR)
|
XP_011531134.1:p.Ala12Val
|
|
|
XM_011532833.1:c.35C>T
(LHCGR)
|
XP_011531135.1:p.Ala12Val
|
|
|
XM_011532834.1:c.8C>T
(LHCGR)
|
XP_011531136.1:p.Ala3Val
|
|
|
XM_005264309.3:c.8C>T
(LHCGR)
|
XP_005264366.1:p.Ala3Val
|
|
|
XM_006712015.3:c.35C>T
(LHCGR)
|
XP_006712078.1:p.Ala12Val
|
|
|
XM_011532834.2:c.8C>T
(LHCGR)
|
XP_011531136.1:p.Ala3Val
|
|
|
XM_017004089.1:c.710C>T
(LHCGR)
|
XP_016859578.1:p.Ala237Val
|
|
|
XM_017004090.1:c.329C>T
(LHCGR)
|
XP_016859579.1:p.Ala110Val
|
|
|
NM_000233.4:c.965C>T
(LHCGR)
MANE Select
|
NP_000224.2:p.Ala322Val
|
|
|
NM_001198593.2:c.3441+17152G>A
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+17152G>A
|
|
