ENST00000262418.12:c.*779G>T
MANE Select
|
ENSP00000262418.6:n.*779G>T
|
|
ENST00000262418.10:c.*779G>T
|
ENSP00000262418.6:n.*779G>T
|
|
ENST00000399246.3:c.*779G>T
|
ENSP00000382190.3:n.*779G>T
|
|
ENST00000631130.1:c.-429G>T
|
ENSP00000486787.1:n.-429G>T
|
|
NM_000342.3:c.*779G>T
|
NP_000333.1:n.*779G>T
|
|
XM_005257593.3:c.*779G>T
|
XP_005257650.1:n.*779G>T
|
|
XM_011525129.1:c.*779G>T
|
XP_011523431.1:n.*779G>T
|
|
XM_005257593.5:c.*779G>T
|
XP_005257650.1:n.*779G>T
|
|
XM_011525129.2:c.*779G>T
|
XP_011523431.1:n.*779G>T
|
|
NM_000342.4:c.*779G>T
MANE Select
|
NP_000333.1:n.*779G>T
|
|