|
ENST00000294954.12:c.1630G>T
(LHCGR)
MANE Select
|
ENSP00000294954.6:p.Ala544Ser
|
|
|
ENST00000294954.11:c.1630G>T
(LHCGR)
|
ENSP00000294954.6:p.Ala544Ser
|
|
|
ENST00000401907.5:c.948-28G>T
(LHCGR)
|
ENSP00000385406.1:n.948-28G>T
|
|
|
ENST00000402114.6:c.3441+16487C>A
(STON1-GTF2A1L)
|
ENSP00000385701.1:n.3441+16487C>A
|
|
|
ENST00000403273.5:c.*374G>T
(LHCGR)
|
ENSP00000385847.1:n.*374G>T
|
|
|
ENST00000405626.5:c.1549G>T
(LHCGR)
|
ENSP00000386033.1:p.Ala517Ser
|
|
|
ENST00000508440.1:c.276+16487C>A
(GTF2A1L)
|
ENSP00000421474.1:n.276+16487C>A
|
|
|
ENST00000602369.3:c.*220+6057G>T
|
ENSP00000473498.1:n.*220+6057G>T
|
|
|
NM_000233.3:c.1630G>T
(LHCGR)
|
NP_000224.2:p.Ala544Ser
|
|
|
NM_001198593.1:c.3441+16487C>A
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16487C>A
|
|
|
XM_005264309.2:c.673G>T
(LHCGR)
|
XP_005264366.1:p.Ala225Ser
|
|
|
XM_006712015.2:c.700G>T
(LHCGR)
|
XP_006712078.1:p.Ala234Ser
|
|
|
XM_011532828.1:c.1555G>T
(LHCGR)
|
XP_011531130.1:p.Ala519Ser
|
|
|
XM_011532829.1:c.1369G>T
(LHCGR)
|
XP_011531131.1:p.Ala457Ser
|
|
|
XM_011532830.1:c.1288G>T
(LHCGR)
|
XP_011531132.1:p.Ala430Ser
|
|
|
XM_011532831.1:c.994G>T
(LHCGR)
|
XP_011531133.1:p.Ala332Ser
|
|
|
XM_011532832.1:c.700G>T
(LHCGR)
|
XP_011531134.1:p.Ala234Ser
|
|
|
XM_011532833.1:c.700G>T
(LHCGR)
|
XP_011531135.1:p.Ala234Ser
|
|
|
XM_011532834.1:c.673G>T
(LHCGR)
|
XP_011531136.1:p.Ala225Ser
|
|
|
XM_005264309.3:c.673G>T
(LHCGR)
|
XP_005264366.1:p.Ala225Ser
|
|
|
XM_006712015.3:c.700G>T
(LHCGR)
|
XP_006712078.1:p.Ala234Ser
|
|
|
XM_011532834.2:c.673G>T
(LHCGR)
|
XP_011531136.1:p.Ala225Ser
|
|
|
XM_017004089.1:c.1375G>T
(LHCGR)
|
XP_016859578.1:p.Ala459Ser
|
|
|
XM_017004090.1:c.994G>T
(LHCGR)
|
XP_016859579.1:p.Ala332Ser
|
|
|
NM_000233.4:c.1630G>T
(LHCGR)
MANE Select
|
NP_000224.2:p.Ala544Ser
|
|
|
NM_001198593.2:c.3441+16487C>A
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16487C>A
|
|
