|
ENST00000294954.12:c.1417C>G
(LHCGR)
MANE Select
|
ENSP00000294954.6:p.His473Asp
|
|
|
ENST00000294954.11:c.1417C>G
(LHCGR)
|
ENSP00000294954.6:p.His473Asp
|
|
|
ENST00000401907.5:c.948-241C>G
(LHCGR)
|
ENSP00000385406.1:n.948-241C>G
|
|
|
ENST00000402114.6:c.3441+16700G>C
(STON1-GTF2A1L)
|
ENSP00000385701.1:n.3441+16700G>C
|
|
|
ENST00000403273.5:c.*161C>G
(LHCGR)
|
ENSP00000385847.1:n.*161C>G
|
|
|
ENST00000405626.5:c.1336C>G
(LHCGR)
|
ENSP00000386033.1:p.His446Asp
|
|
|
ENST00000508440.1:c.276+16700G>C
(GTF2A1L)
|
ENSP00000421474.1:n.276+16700G>C
|
|
|
ENST00000602369.3:c.*220+5844C>G
|
ENSP00000473498.1:n.*220+5844C>G
|
|
|
NM_000233.3:c.1417C>G
(LHCGR)
|
NP_000224.2:p.His473Asp
|
|
|
NM_001198593.1:c.3441+16700G>C
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16700G>C
|
|
|
XM_005264309.2:c.460C>G
(LHCGR)
|
XP_005264366.1:p.His154Asp
|
|
|
XM_006712015.2:c.487C>G
(LHCGR)
|
XP_006712078.1:p.His163Asp
|
|
|
XM_011532828.1:c.1342C>G
(LHCGR)
|
XP_011531130.1:p.His448Asp
|
|
|
XM_011532829.1:c.1156C>G
(LHCGR)
|
XP_011531131.1:p.His386Asp
|
|
|
XM_011532830.1:c.1075C>G
(LHCGR)
|
XP_011531132.1:p.His359Asp
|
|
|
XM_011532831.1:c.781C>G
(LHCGR)
|
XP_011531133.1:p.His261Asp
|
|
|
XM_011532832.1:c.487C>G
(LHCGR)
|
XP_011531134.1:p.His163Asp
|
|
|
XM_011532833.1:c.487C>G
(LHCGR)
|
XP_011531135.1:p.His163Asp
|
|
|
XM_011532834.1:c.460C>G
(LHCGR)
|
XP_011531136.1:p.His154Asp
|
|
|
XM_005264309.3:c.460C>G
(LHCGR)
|
XP_005264366.1:p.His154Asp
|
|
|
XM_006712015.3:c.487C>G
(LHCGR)
|
XP_006712078.1:p.His163Asp
|
|
|
XM_011532834.2:c.460C>G
(LHCGR)
|
XP_011531136.1:p.His154Asp
|
|
|
XM_017004089.1:c.1162C>G
(LHCGR)
|
XP_016859578.1:p.His388Asp
|
|
|
XM_017004090.1:c.781C>G
(LHCGR)
|
XP_016859579.1:p.His261Asp
|
|
|
NM_000233.4:c.1417C>G
(LHCGR)
MANE Select
|
NP_000224.2:p.His473Asp
|
|
|
NM_001198593.2:c.3441+16700G>C
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16700G>C
|
|
