ENST00000265572.8:c.*33G>T
MANE Select
|
ENSP00000265572.3:n.*33G>T
|
|
ENST00000673285.2:c.1176G>T
|
ENSP00000500765.2:p.Ser392=
|
|
ENST00000265572.7:c.*33G>T
|
ENSP00000265572.3:n.*33G>T
|
|
ENST00000520287.5:c.*33G>T
|
ENSP00000429706.1:n.*33G>T
|
|
ENST00000522508.1:c.*999G>T
|
ENSP00000428231.1:n.*999G>T
|
|
ENST00000524278.5:c.*33G>T
|
ENSP00000430923.1:n.*33G>T
|
|
ENST00000612786.4:c.*33G>T
|
ENSP00000483000.1:n.*33G>T
|
|
ENST00000613482.1:c.1134G>T
|
ENSP00000478453.1:n.1134G>T
|
|
NM_000912.3:c.*33G>T
|
NP_000903.2:n.*33G>T
|
|
NM_001282904.1:c.*33G>T
|
NP_001269833.1:n.*33G>T
|
|
NM_000912.4:c.*33G>T
|
NP_000903.2:n.*33G>T
|
|
NM_001318497.1:c.1176G>T
|
NP_001305426.1:p.Ser392=
|
|
NM_000912.5:c.*33G>T
MANE Select
|
NP_000903.2:n.*33G>T
|
|
NM_001318497.2:c.1176G>T
|
NP_001305426.1:p.Ser392=
|
|
NM_001282904.2:c.*33G>T
|
NP_001269833.1:n.*33G>T
|
|