|
ENST00000294954.12:c.1958G>T
(LHCGR)
MANE Select
|
ENSP00000294954.6:p.Arg653Met
|
|
|
ENST00000294954.11:c.1958G>T
(LHCGR)
|
ENSP00000294954.6:p.Arg653Met
|
|
|
ENST00000401907.5:c.*270G>T
(LHCGR)
|
ENSP00000385406.1:n.*270G>T
|
|
|
ENST00000402114.6:c.3441+16159C>A
(STON1-GTF2A1L)
|
ENSP00000385701.1:n.3441+16159C>A
|
|
|
ENST00000403273.5:c.*702G>T
(LHCGR)
|
ENSP00000385847.1:n.*702G>T
|
|
|
ENST00000405626.5:c.1877G>T
(LHCGR)
|
ENSP00000386033.1:p.Arg626Met
|
|
|
ENST00000508440.1:c.276+16159C>A
(GTF2A1L)
|
ENSP00000421474.1:n.276+16159C>A
|
|
|
ENST00000602369.3:c.*220+6385G>T
|
ENSP00000473498.1:n.*220+6385G>T
|
|
|
NM_000233.3:c.1958G>T
(LHCGR)
|
NP_000224.2:p.Arg653Met
|
|
|
NM_001198593.1:c.3441+16159C>A
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16159C>A
|
|
|
XM_005264309.2:c.1001G>T
(LHCGR)
|
XP_005264366.1:p.Arg334Met
|
|
|
XM_006712015.2:c.1028G>T
(LHCGR)
|
XP_006712078.1:p.Arg343Met
|
|
|
XM_011532828.1:c.1883G>T
(LHCGR)
|
XP_011531130.1:p.Arg628Met
|
|
|
XM_011532829.1:c.1697G>T
(LHCGR)
|
XP_011531131.1:p.Arg566Met
|
|
|
XM_011532830.1:c.1616G>T
(LHCGR)
|
XP_011531132.1:p.Arg539Met
|
|
|
XM_011532831.1:c.1322G>T
(LHCGR)
|
XP_011531133.1:p.Arg441Met
|
|
|
XM_011532832.1:c.1028G>T
(LHCGR)
|
XP_011531134.1:p.Arg343Met
|
|
|
XM_011532833.1:c.1028G>T
(LHCGR)
|
XP_011531135.1:p.Arg343Met
|
|
|
XM_011532834.1:c.1001G>T
(LHCGR)
|
XP_011531136.1:p.Arg334Met
|
|
|
XM_005264309.3:c.1001G>T
(LHCGR)
|
XP_005264366.1:p.Arg334Met
|
|
|
XM_006712015.3:c.1028G>T
(LHCGR)
|
XP_006712078.1:p.Arg343Met
|
|
|
XM_011532834.2:c.1001G>T
(LHCGR)
|
XP_011531136.1:p.Arg334Met
|
|
|
XM_017004089.1:c.1703G>T
(LHCGR)
|
XP_016859578.1:p.Arg568Met
|
|
|
XM_017004090.1:c.1322G>T
(LHCGR)
|
XP_016859579.1:p.Arg441Met
|
|
|
NM_000233.4:c.1958G>T
(LHCGR)
MANE Select
|
NP_000224.2:p.Arg653Met
|
|
|
NM_001198593.2:c.3441+16159C>A
(STON1-GTF2A1L)
|
NP_001185522.1:n.3441+16159C>A
|
|
