ENST00000348974.5:c.*2-381G>T
|
ENSP00000330021.7:n.*2-381G>T
|
|
ENST00000394236.9:c.*451G>T
MANE Select
|
ENSP00000377783.3:n.*451G>T
|
|
ENST00000407433.6:c.*451G>T
|
ENSP00000385794.2:n.*451G>T
|
|
ENST00000647936.1:c.*585G>T
|
ENSP00000496822.1:n.*585G>T
|
|
ENST00000648381.1:n.2650G>T
|
|
|
ENST00000648853.1:c.*451G>T
|
ENSP00000497262.1:n.*451G>T
|
|
ENST00000650591.1:c.*451G>T
|
ENSP00000497376.1:n.*451G>T
|
|
ENST00000394236.7:c.*451G>T
|
ENSP00000377783.3:n.*451G>T
|
|
ENST00000407433.5:c.*451G>T
|
ENSP00000385794.1:n.*451G>T
|
|
NM_000313.3:c.*451G>T , LRG_572t1:c.*451G>T
|
NP_000304.2:n.*451G>T
|
|
NM_001314077.1:c.*451G>T , LRG_572t2:c.*451G>T
|
NP_001301006.1:n.*451G>T
|
|
NM_000313.4:c.*451G>T
MANE Select
|
NP_000304.2:n.*451G>T
|
|
NM_001314077.2:c.*451G>T
|
NP_001301006.1:n.*451G>T
|
|