ENST00000294288.5:c.525C>G
MANE Select
|
ENSP00000294288.4:p.Gly175=
|
|
ENST00000545205.2:c.*310C>G
|
ENSP00000446180.1:n.*310C>G
|
|
ENST00000636477.1:c.477C>G
|
ENSP00000490746.1:p.Gly159=
|
|
ENST00000294288.4:c.525C>G
|
ENSP00000294288.4:p.Gly175=
|
|
ENST00000353903.9:c.354C>G
|
ENSP00000312037.4:p.Gly118=
|
|
ENST00000545205.1:c.*310C>G
|
ENSP00000446180.1:n.*310C>G
|
|
NM_016366.2:c.525C>G
|
NP_057450.2:p.Gly175=
|
|
XM_005274046.1:c.543C>G
|
XP_005274103.1:p.Gly181=
|
|
NM_001318496.1:c.543C>G
|
NP_001305425.1:p.Gly181=
|
|
NM_001318496.2:c.543C>G
|
NP_001305425.1:p.Gly181=
|
|
NM_016366.3:c.525C>G
MANE Select
|
NP_057450.2:p.Gly175=
|
|