|
ENST00000335542.13:c.111G>T
(GHRL)
MANE Select
|
ENSP00000335074.8:p.Gln37His
|
|
|
ENST00000287656.11:c.109-1G>T
(GHRL)
|
ENSP00000287656.7:n.109-1G>T
|
|
|
ENST00000335542.12:c.111G>T
(GHRL)
|
ENSP00000335074.8:p.Gln37His
|
|
|
ENST00000422159.5:c.111G>T
(GHRL)
|
ENSP00000405464.1:p.Gln37His
|
|
|
ENST00000429122.1:c.111G>T
(GHRL)
|
ENSP00000414819.1:p.Gln37His
|
|
|
ENST00000430179.5:c.109-1G>T
(GHRL)
|
ENSP00000399922.1:n.109-1G>T
|
|
|
ENST00000437422.6:c.75G>T
(GHRL)
|
ENSP00000416768.2:p.Gln25His
|
|
|
ENST00000439975.6:c.72+2966G>T
(GHRL)
|
ENSP00000403725.2:n.72+2966G>T
|
|
|
ENST00000446937.2:c.72+2966G>T
(GHRL)
|
ENSP00000394923.2:n.72+2966G>T
|
|
|
ENST00000449238.6:c.73-1G>T
(GHRL)
|
ENSP00000388145.2:n.73-1G>T
|
|
|
ENST00000457360.5:c.111G>T
(GHRL)
|
ENSP00000391406.1:p.Gln37His
|
|
|
ENST00000481287.5:n.288G>T
(GHRL)
|
|
|
|
ENST00000491589.5:n.202G>T
(GHRL)
|
|
|
|
NM_001134941.2:c.109-1G>T
(GHRL)
|
NP_001128413.1:n.109-1G>T
|
|
|
NM_001134944.1:c.75G>T
(GHRL)
|
NP_001128416.1:p.Gln25His
|
|
|
NM_001134945.1:c.73-1G>T
(GHRL)
|
NP_001128417.1:n.73-1G>T
|
|
|
NM_001134946.1:c.72+2966G>T
(GHRL)
|
NP_001128418.1:n.72+2966G>T
|
|
|
NM_001302821.1:c.111G>T
(GHRL)
|
NP_001289750.1:p.Gln37His
|
|
|
NM_001302822.1:c.111G>T
(GHRL)
|
NP_001289751.1:p.Gln37His
|
|
|
NM_001302823.1:c.109-1G>T
(GHRL)
|
NP_001289752.1:n.109-1G>T
|
|
|
NM_001302824.1:c.111G>T
(GHRL)
|
NP_001289753.1:p.Gln37His
|
|
|
NM_001302825.1:c.111G>T
(GHRL)
|
NP_001289754.1:p.Gln37His
|
|
|
NM_016362.4:c.111G>T
(GHRL)
|
NP_057446.1:p.Gln37His
|
|
|
NR_004431.3:n.383+1774C>A
(GHRLOS)
|
|
|
|
NR_024144.2:n.466+1774C>A
(GHRLOS)
|
|
|
|
NR_024145.2:n.555+1774C>A
(GHRLOS)
|
|
|
|
NR_073566.1:n.566+1770C>A
(GHRLOS)
|
|
|
|
NR_073567.1:n.554+1774C>A
(GHRLOS)
|
|
|
|
NR_073568.1:n.409+1774C>A
(GHRLOS)
|
|
|
|
NR_126505.1:n.106+2966G>T
(GHRL)
|
|
|
|
XM_017006612.2:c.111G>T
(GHRL)
|
XP_016862101.1:p.Gln37His
|
|
|
XM_017006613.2:c.109-1G>T
(GHRL)
|
XP_016862102.1:n.109-1G>T
|
|
|
XM_024453594.1:c.111G>T
(GHRL)
|
XP_024309362.1:p.Gln37His
|
|
|
NM_001134941.3:c.109-1G>T
(GHRL)
|
NP_001128413.1:n.109-1G>T
|
|
|
NM_001134944.2:c.75G>T
(GHRL)
|
NP_001128416.1:p.Gln25His
|
|
|
NM_001134945.2:c.73-1G>T
(GHRL)
|
NP_001128417.1:n.73-1G>T
|
|
|
NM_001134946.2:c.72+2966G>T
(GHRL)
|
NP_001128418.1:n.72+2966G>T
|
|
|
NM_001302821.2:c.111G>T
(GHRL)
|
NP_001289750.1:p.Gln37His
|
|
|
NM_001302822.2:c.111G>T
(GHRL)
|
NP_001289751.1:p.Gln37His
|
|
|
NM_001302823.2:c.109-1G>T
(GHRL)
|
NP_001289752.1:n.109-1G>T
|
|
|
NM_001302824.2:c.111G>T
(GHRL)
|
NP_001289753.1:p.Gln37His
|
|
|
NM_001302825.2:c.111G>T
(GHRL)
|
NP_001289754.1:p.Gln37His
|
|
|
NM_016362.5:c.111G>T
(GHRL)
MANE Select
|
NP_057446.1:p.Gln37His
|
|
|
NR_126505.2:n.106+2966G>T
(GHRL)
|
|
|
