ENST00000294954.12:c.1449_1463delinsCATTCTGATTATGCT
(LHCGR)
MANE Select
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ENSP00000294954.6:p.Ala483=
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ENST00000294954.11:c.1449_1463delinsCATTCTGATTATGCT
(LHCGR)
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ENSP00000294954.6:p.Ala483=
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ENST00000401907.5:c.948-209_948-195delinsCATTCTGATTATGCT
(LHCGR)
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ENSP00000385406.1:n.948-209_948-195delins...
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ENST00000402114.6:c.3441+16654_3441+16668delinsAGCATAATCAGAATG
(STON1-GTF2A1L)
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ENSP00000385701.1:n.3441+16654_3441+16668...
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ENST00000403273.5:c.*193_*207delinsCATTCTGATTATGCT
(LHCGR)
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ENSP00000385847.1:n.*193_*207delinsCATTCT...
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ENST00000405626.5:c.1368_1382delinsCATTCTGATTATGCT
(LHCGR)
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ENSP00000386033.1:p.Ala456=
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ENST00000508440.1:c.276+16654_276+16668delinsAGCATAATCAGAATG
(GTF2A1L)
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ENSP00000421474.1:n.276+16654_276+16668de...
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ENST00000602369.3:c.*220+5876_*220+5890delinsCATTCTGATTATGCT
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ENSP00000473498.1:n.*220+5876_*220+5890de...
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NM_000233.3:c.1449_1463delinsCATTCTGATTATGCT
(LHCGR)
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NP_000224.2:p.Ala483=
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NM_001198593.1:c.3441+16654_3441+16668delinsAGCATAATCAGAATG
(STON1-GTF2A1L)
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NP_001185522.1:n.3441+16654_3441+16668del...
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XM_005264309.2:c.492_506delinsCATTCTGATTATGCT
(LHCGR)
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XP_005264366.1:p.Ala164=
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XM_006712015.2:c.519_533delinsCATTCTGATTATGCT
(LHCGR)
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XP_006712078.1:p.Ala173=
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XM_011532828.1:c.1374_1388delinsCATTCTGATTATGCT
(LHCGR)
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XP_011531130.1:p.Ala458=
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XM_011532829.1:c.1188_1202delinsCATTCTGATTATGCT
(LHCGR)
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XP_011531131.1:p.Ala396=
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XM_011532830.1:c.1107_1121delinsCATTCTGATTATGCT
(LHCGR)
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XP_011531132.1:p.Ala369=
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XM_011532831.1:c.813_827delinsCATTCTGATTATGCT
(LHCGR)
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XP_011531133.1:p.Ala271=
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XM_011532832.1:c.519_533delinsCATTCTGATTATGCT
(LHCGR)
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XP_011531134.1:p.Ala173=
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XM_011532833.1:c.519_533delinsCATTCTGATTATGCT
(LHCGR)
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XP_011531135.1:p.Ala173=
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XM_011532834.1:c.492_506delinsCATTCTGATTATGCT
(LHCGR)
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XP_011531136.1:p.Ala164=
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XM_005264309.3:c.492_506delinsCATTCTGATTATGCT
(LHCGR)
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XP_005264366.1:p.Ala164=
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XM_006712015.3:c.519_533delinsCATTCTGATTATGCT
(LHCGR)
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XP_006712078.1:p.Ala173=
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XM_011532834.2:c.492_506delinsCATTCTGATTATGCT
(LHCGR)
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XP_011531136.1:p.Ala164=
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XM_017004089.1:c.1194_1208delinsCATTCTGATTATGCT
(LHCGR)
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XP_016859578.1:p.Ala398=
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XM_017004090.1:c.813_827delinsCATTCTGATTATGCT
(LHCGR)
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XP_016859579.1:p.Ala271=
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NM_000233.4:c.1449_1463delinsCATTCTGATTATGCT
(LHCGR)
MANE Select
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NP_000224.2:p.Ala483=
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NM_001198593.2:c.3441+16654_3441+16668delinsAGCATAATCAGAATG
(STON1-GTF2A1L)
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NP_001185522.1:n.3441+16654_3441+16668del...
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