|
ENST00000294954.12:c.980G>A
(LHCGR)
MANE Select
|
ENSP00000294954.6:p.Ser327Asn
|
|
|
ENST00000294954.11:c.980G>A
(LHCGR)
|
ENSP00000294954.6:p.Ser327Asn
|
|
|
ENST00000401907.5:c.948-678G>A
(LHCGR)
|
ENSP00000385406.1:n.948-678G>A
|
|
|
ENST00000402114.6:c.3441+17137C>T
(STON1-GTF2A1L)
|
ENSP00000385701.1:n.3441+17137C>T
|
|
|
ENST00000403273.5:c.948-234G>A
(LHCGR)
|
ENSP00000385847.1:n.948-234G>A
|
|
|
ENST00000405626.5:c.899G>A
(LHCGR)
|
ENSP00000386033.1:p.Ser300Asn
|
|
|
ENST00000508440.1:c.276+17137C>T
(GTF2A1L)
|
ENSP00000421474.1:n.276+17137C>T
|
|
|
ENST00000602369.3:c.*220+5407G>A
|
ENSP00000473498.1:n.*220+5407G>A
|
|
|
NM_000233.3:c.980G>A
(LHCGR)
|
NP_000224.2:p.Ser327Asn
|
|
|
NM_001198593.1:c.3441+17137C>T
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+17137C>T
|
|
|
XM_005264309.2:c.23G>A
(LHCGR)
|
XP_005264366.1:p.Ser8Asn
|
|
|
XM_006712015.2:c.50G>A
(LHCGR)
|
XP_006712078.1:p.Ser17Asn
|
|
|
XM_011532828.1:c.905G>A
(LHCGR)
|
XP_011531130.1:p.Ser302Asn
|
|
|
XM_011532829.1:c.719G>A
(LHCGR)
|
XP_011531131.1:p.Ser240Asn
|
|
|
XM_011532830.1:c.638G>A
(LHCGR)
|
XP_011531132.1:p.Ser213Asn
|
|
|
XM_011532831.1:c.344G>A
(LHCGR)
|
XP_011531133.1:p.Ser115Asn
|
|
|
XM_011532832.1:c.50G>A
(LHCGR)
|
XP_011531134.1:p.Ser17Asn
|
|
|
XM_011532833.1:c.50G>A
(LHCGR)
|
XP_011531135.1:p.Ser17Asn
|
|
|
XM_011532834.1:c.23G>A
(LHCGR)
|
XP_011531136.1:p.Ser8Asn
|
|
|
XM_005264309.3:c.23G>A
(LHCGR)
|
XP_005264366.1:p.Ser8Asn
|
|
|
XM_006712015.3:c.50G>A
(LHCGR)
|
XP_006712078.1:p.Ser17Asn
|
|
|
XM_011532834.2:c.23G>A
(LHCGR)
|
XP_011531136.1:p.Ser8Asn
|
|
|
XM_017004089.1:c.725G>A
(LHCGR)
|
XP_016859578.1:p.Ser242Asn
|
|
|
XM_017004090.1:c.344G>A
(LHCGR)
|
XP_016859579.1:p.Ser115Asn
|
|
|
NM_000233.4:c.980G>A
(LHCGR)
MANE Select
|
NP_000224.2:p.Ser327Asn
|
|
|
NM_001198593.2:c.3441+17137C>T
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+17137C>T
|
|
