ENST00000323322.10:c.382G>A
(GH1)
MANE Select
|
ENSP00000312673.5:p.Val128Met
|
|
ENST00000647774.1:c.660G>A
|
|
|
ENST00000323322.9:c.382G>A
(GH1)
|
ENSP00000312673.5:p.Val128Met
|
|
ENST00000342364.8:c.172-328G>A
(GH1)
|
ENSP00000339278.4:n.172-328G>A
|
|
ENST00000351388.8:c.262G>A
(GH1)
|
ENSP00000343791.4:p.Val88Met
|
|
ENST00000392824.8:c.10+933G>A
(CSHL1)
|
ENSP00000376569.5:n.10+933G>A
|
|
ENST00000458650.6:c.337G>A
(GH1)
|
ENSP00000408486.2:p.Val113Met
|
|
ENST00000579711.1:n.743G>A
(GH1)
|
|
|
ENST00000617086.1:c.11-328G>A
(GH1)
|
ENSP00000481276.1:n.11-328G>A
|
|
NM_000515.4:c.382G>A
(GH1)
|
NP_000506.2:p.Val128Met
|
|
NM_022559.3:c.337G>A
(GH1)
|
NP_072053.1:p.Val113Met
|
|
NM_022560.3:c.262G>A
(GH1)
|
NP_072054.1:p.Val88Met
|
|
XM_011524612.1:c.382G>A
(GH1)
|
XP_011522914.1:p.Val128Met
|
|
XR_002958148.1:n.433C>T
|
|
|
NM_000515.5:c.382G>A
(GH1)
MANE Select
|
NP_000506.2:p.Val128Met
|
|
NM_022559.4:c.337G>A
(GH1)
|
NP_072053.1:p.Val113Met
|
|
NM_022560.4:c.262G>A
(GH1)
|
NP_072054.1:p.Val88Met
|
|