ENST00000340855.11:c.1007-181A>T
MANE Select
|
ENSP00000339801.6:n.1007-181A>T
|
|
ENST00000651111.1:c.374-181A>T
|
ENSP00000498395.1:n.374-181A>T
|
|
ENST00000340855.10:c.1007-181A>T
|
ENSP00000339801.6:n.1007-181A>T
|
|
ENST00000370441.8:c.*9A>T
|
ENSP00000359470.4:n.*9A>T
|
|
ENST00000422081.6:c.374-181A>T
|
ENSP00000477056.1:n.374-181A>T
|
|
ENST00000441880.1:n.114-181A>T
|
|
|
ENST00000466323.5:c.*232A>T
|
ENSP00000418264.1:n.*232A>T
|
|
ENST00000490775.5:n.826A>T
|
|
|
NM_000202.6:c.1007-181A>T
|
NP_000193.1:n.1007-181A>T
|
|
NM_001166550.2:c.737-181A>T
|
NP_001160022.1:n.737-181A>T
|
|
NM_006123.4:c.*9A>T
|
NP_006114.1:n.*9A>T
|
|
NR_104128.1:n.1388A>T
|
|
|
NM_000202.7:c.1007-181A>T
|
NP_000193.1:n.1007-181A>T
|
|
NM_001166550.3:c.737-181A>T
|
NP_001160022.1:n.737-181A>T
|
|
NM_000202.8:c.1007-181A>T
MANE Select
|
NP_000193.1:n.1007-181A>T
|
|
NM_001166550.4:c.737-181A>T
|
NP_001160022.1:n.737-181A>T
|
|
NM_006123.5:c.*9A>T
|
NP_006114.1:n.*9A>T
|
|
NR_104128.2:n.1340A>T
|
|
|