ENST00000323322.10:c.432G>T
(GH1)
MANE Select
|
ENSP00000312673.5:p.Glu144Asp
|
|
ENST00000647774.1:c.710G>T
|
|
|
ENST00000323322.9:c.432G>T
(GH1)
|
ENSP00000312673.5:p.Glu144Asp
|
|
ENST00000342364.8:c.172-278G>T
(GH1)
|
ENSP00000339278.4:n.172-278G>T
|
|
ENST00000351388.8:c.312G>T
(GH1)
|
ENSP00000343791.4:p.Glu104Asp
|
|
ENST00000392824.8:c.10+983G>T
(CSHL1)
|
ENSP00000376569.5:n.10+983G>T
|
|
ENST00000458650.6:c.387G>T
(GH1)
|
ENSP00000408486.2:p.Glu129Asp
|
|
ENST00000579711.1:n.793G>T
(GH1)
|
|
|
ENST00000617086.1:c.11-278G>T
(GH1)
|
ENSP00000481276.1:n.11-278G>T
|
|
NM_000515.4:c.432G>T
(GH1)
|
NP_000506.2:p.Glu144Asp
|
|
NM_022559.3:c.387G>T
(GH1)
|
NP_072053.1:p.Glu129Asp
|
|
NM_022560.3:c.312G>T
(GH1)
|
NP_072054.1:p.Glu104Asp
|
|
XM_011524612.1:c.432G>T
(GH1)
|
XP_011522914.1:p.Glu144Asp
|
|
XR_002958148.1:n.389-6C>A
|
|
|
NM_000515.5:c.432G>T
(GH1)
MANE Select
|
NP_000506.2:p.Glu144Asp
|
|
NM_022559.4:c.387G>T
(GH1)
|
NP_072053.1:p.Glu129Asp
|
|
NM_022560.4:c.312G>T
(GH1)
|
NP_072054.1:p.Glu104Asp
|
|