ENST00000348974.5:c.966-42G>T
|
ENSP00000330021.7:n.966-42G>T
|
|
ENST00000394236.9:c.966-42G>T
MANE Select
|
ENSP00000377783.3:n.966-42G>T
|
|
ENST00000407433.6:c.921-42G>T
|
ENSP00000385794.2:n.921-42G>T
|
|
ENST00000647936.1:c.966-42G>T
|
ENSP00000496822.1:n.966-42G>T
|
|
ENST00000648381.1:n.1134-42G>T
|
|
|
ENST00000648853.1:c.924-42G>T
|
ENSP00000497262.1:n.924-42G>T
|
|
ENST00000649103.1:c.1065-42G>T
|
ENSP00000497962.1:n.1065-42G>T
|
|
ENST00000650591.1:c.1062-42G>T
|
ENSP00000497376.1:n.1062-42G>T
|
|
ENST00000394236.7:c.966-42G>T
|
ENSP00000377783.3:n.966-42G>T
|
|
ENST00000407433.5:c.573-42G>T
|
ENSP00000385794.1:n.573-42G>T
|
|
NM_000313.3:c.966-42G>T , LRG_572t1:c.966-42G>T
|
NP_000304.2:n.966-42G>T
|
|
NM_001314077.1:c.1062-42G>T , LRG_572t2:c.1062-42G>T
|
NP_001301006.1:n.1062-42G>T
|
|
NM_000313.4:c.966-42G>T
MANE Select
|
NP_000304.2:n.966-42G>T
|
|
NM_001314077.2:c.1062-42G>T
|
NP_001301006.1:n.1062-42G>T
|
|