ENST00000294288.5:c.456C>T
MANE Select
|
ENSP00000294288.4:p.Ile152=
|
|
ENST00000545205.2:c.*241C>T
|
ENSP00000446180.1:n.*241C>T
|
|
ENST00000636477.1:c.408C>T
|
ENSP00000490746.1:p.Ile136=
|
|
ENST00000294288.4:c.456C>T
|
ENSP00000294288.4:p.Ile152=
|
|
ENST00000353903.9:c.285C>T
|
ENSP00000312037.4:p.Ile95=
|
|
ENST00000545205.1:c.*241C>T
|
ENSP00000446180.1:n.*241C>T
|
|
NM_016366.2:c.456C>T
|
NP_057450.2:p.Ile152=
|
|
XM_005274046.1:c.474C>T
|
XP_005274103.1:p.Ile158=
|
|
NM_001318496.1:c.474C>T
|
NP_001305425.1:p.Ile158=
|
|
NM_001318496.2:c.474C>T
|
NP_001305425.1:p.Ile158=
|
|
NM_016366.3:c.456C>T
MANE Select
|
NP_057450.2:p.Ile152=
|
|