ENST00000442544.7:c.564A>G
MANE Select
|
ENSP00000389140.2:p.Arg188=
|
|
ENST00000304775.12:c.365A>G
|
|
|
ENST00000412726.5:c.495A>G
|
ENSP00000397322.2:p.Arg165=
|
|
ENST00000442544.6:c.564A>G
|
ENSP00000389140.2:p.Arg188=
|
|
ENST00000579349.1:c.485A>G
|
|
|
ENST00000580024.1:n.477A>G
|
|
|
ENST00000581559.1:c.485A>G
|
ENSP00000463463.1:n.485A>G
|
|
NM_005215.3:c.564A>G
|
NP_005206.2:p.Arg188=
|
|
XM_011525843.1:c.564A>G
|
XP_011524145.1:p.Arg188=
|
|
XM_011525845.1:c.564A>G
|
XP_011524147.1:p.Arg188=
|
|
XM_011525846.1:c.564A>G
|
XP_011524148.1:p.Arg188=
|
|
XM_017025568.1:c.564A>G
|
XP_016881057.1:p.Arg188=
|
|
XM_017025569.1:c.564A>G
|
XP_016881058.1:p.Arg188=
|
|
NM_005215.4:c.564A>G
MANE Select
|
NP_005206.2:p.Arg188=
|
|