ENST00000323322.10:c.385T>C
(GH1)
MANE Select
|
ENSP00000312673.5:p.Tyr129His
|
|
ENST00000647774.1:c.663T>C
|
|
|
ENST00000323322.9:c.385T>C
(GH1)
|
ENSP00000312673.5:p.Tyr129His
|
|
ENST00000342364.8:c.172-325T>C
(GH1)
|
ENSP00000339278.4:n.172-325T>C
|
|
ENST00000351388.8:c.265T>C
(GH1)
|
ENSP00000343791.4:p.Tyr89His
|
|
ENST00000392824.8:c.10+936T>C
(CSHL1)
|
ENSP00000376569.5:n.10+936T>C
|
|
ENST00000458650.6:c.340T>C
(GH1)
|
ENSP00000408486.2:p.Tyr114His
|
|
ENST00000579711.1:n.746T>C
(GH1)
|
|
|
ENST00000617086.1:c.11-325T>C
(GH1)
|
ENSP00000481276.1:n.11-325T>C
|
|
NM_000515.4:c.385T>C
(GH1)
|
NP_000506.2:p.Tyr129His
|
|
NM_022559.3:c.340T>C
(GH1)
|
NP_072053.1:p.Tyr114His
|
|
NM_022560.3:c.265T>C
(GH1)
|
NP_072054.1:p.Tyr89His
|
|
XM_011524612.1:c.385T>C
(GH1)
|
XP_011522914.1:p.Tyr129His
|
|
XR_002958148.1:n.430A>G
|
|
|
NM_000515.5:c.385T>C
(GH1)
MANE Select
|
NP_000506.2:p.Tyr129His
|
|
NM_022559.4:c.340T>C
(GH1)
|
NP_072053.1:p.Tyr114His
|
|
NM_022560.4:c.265T>C
(GH1)
|
NP_072054.1:p.Tyr89His
|
|