ENST00000340855.11:c.1007-187T>C
MANE Select
|
ENSP00000339801.6:n.1007-187T>C
|
|
ENST00000651111.1:c.374-187T>C
|
ENSP00000498395.1:n.374-187T>C
|
|
ENST00000340855.10:c.1007-187T>C
|
ENSP00000339801.6:n.1007-187T>C
|
|
ENST00000370441.8:c.*3T>C
|
ENSP00000359470.4:n.*3T>C
|
|
ENST00000422081.6:c.374-187T>C
|
ENSP00000477056.1:n.374-187T>C
|
|
ENST00000441880.1:n.114-187T>C
|
|
|
ENST00000466323.5:c.*226T>C
|
ENSP00000418264.1:n.*226T>C
|
|
ENST00000490775.5:n.820T>C
|
|
|
NM_000202.6:c.1007-187T>C
|
NP_000193.1:n.1007-187T>C
|
|
NM_001166550.2:c.737-187T>C
|
NP_001160022.1:n.737-187T>C
|
|
NM_006123.4:c.*3T>C
|
NP_006114.1:n.*3T>C
|
|
NR_104128.1:n.1382T>C
|
|
|
NM_000202.7:c.1007-187T>C
|
NP_000193.1:n.1007-187T>C
|
|
NM_001166550.3:c.737-187T>C
|
NP_001160022.1:n.737-187T>C
|
|
NM_000202.8:c.1007-187T>C
MANE Select
|
NP_000193.1:n.1007-187T>C
|
|
NM_001166550.4:c.737-187T>C
|
NP_001160022.1:n.737-187T>C
|
|
NM_006123.5:c.*3T>C
|
NP_006114.1:n.*3T>C
|
|
NR_104128.2:n.1334T>C
|
|
|