|
NM_024529.5:c.1511G>A
MANE Select
|
NP_078805.3:p.Arg504His
|
|
ENST00000367435.5:c.1511G>A
MANE Select
|
ENSP00000356405.4:p.Arg504His
|
|
NM_024529.4:c.1511G>A , LRG_507t1:c.1511G>A
|
NP_078805.3:p.Arg504His
|
|
ENST00000367435.3:c.1511G>A
|
ENSP00000356405.3:p.Arg504His
|
|
ENST00000477868.1:n.223G>A
|
|
|
ENST00000635846.1:c.1268G>A
|
ENSP00000490035.1:p.Arg423His
|
|
ENST00000643006.1:c.*421G>A
|
ENSP00000496633.1:n.*421G>A
|
|
ENST00000648071.1:c.*1487G>A
|
ENSP00000497513.1:n.*1487G>A
|
|
ENST00000649613.1:n.761G>A
|
|
|
ENST00000650197.1:c.*209G>A
|
ENSP00000496929.1:n.*209G>A
|