ENST00000323322.10:c.423G>A
(GH1)
MANE Select
|
ENSP00000312673.5:p.Lys141=
|
|
ENST00000647774.1:c.701G>A
|
|
|
ENST00000323322.9:c.423G>A
(GH1)
|
ENSP00000312673.5:p.Lys141=
|
|
ENST00000342364.8:c.172-287G>A
(GH1)
|
ENSP00000339278.4:n.172-287G>A
|
|
ENST00000351388.8:c.303G>A
(GH1)
|
ENSP00000343791.4:p.Lys101=
|
|
ENST00000392824.8:c.10+974G>A
(CSHL1)
|
ENSP00000376569.5:n.10+974G>A
|
|
ENST00000458650.6:c.378G>A
(GH1)
|
ENSP00000408486.2:p.Lys126=
|
|
ENST00000579711.1:n.784G>A
(GH1)
|
|
|
ENST00000617086.1:c.11-287G>A
(GH1)
|
ENSP00000481276.1:n.11-287G>A
|
|
NM_000515.4:c.423G>A
(GH1)
|
NP_000506.2:p.Lys141=
|
|
NM_022559.3:c.378G>A
(GH1)
|
NP_072053.1:p.Lys126=
|
|
NM_022560.3:c.303G>A
(GH1)
|
NP_072054.1:p.Lys101=
|
|
XM_011524612.1:c.423G>A
(GH1)
|
XP_011522914.1:p.Lys141=
|
|
XR_002958148.1:n.392C>T
|
|
|
NM_000515.5:c.423G>A
(GH1)
MANE Select
|
NP_000506.2:p.Lys141=
|
|
NM_022559.4:c.378G>A
(GH1)
|
NP_072053.1:p.Lys126=
|
|
NM_022560.4:c.303G>A
(GH1)
|
NP_072054.1:p.Lys101=
|
|