ENST00000509700.2:c.671+757G>T
|
|
|
ENST00000636689.1:n.95-1729G>T
|
|
|
ENST00000637644.1:c.487+969G>T
|
ENSP00000490282.1:n.487+969G>T
|
|
ENST00000638728.1:c.*316G>T
|
ENSP00000492619.1:n.*316G>T
|
|
ENST00000638840.1:c.919+259G>T
|
|
|
ENST00000638868.1:c.*316G>T
|
ENSP00000491250.1:n.*316G>T
|
|
ENST00000639408.1:c.488-476G>T
|
ENSP00000491635.1:n.488-476G>T
|
|
ENST00000640017.1:c.670-476G>T
|
ENSP00000491337.1:n.670-476G>T
|
|
ENST00000640914.1:c.125-476G>T
|
|
|
ENST00000644903.1:c.*316G>T
MANE Select
|
ENSP00000495557.1:n.*316G>T
|
|
ENST00000368089.3:c.*316G>T
|
ENSP00000357068.3:n.*316G>T
|
|
ENST00000509700.1:n.463-476G>T
|
|
|
NM_002241.4:c.*316G>T
|
NP_002232.2:n.*316G>T
|
|
NM_002241.5:c.*316G>T
MANE Select
|
NP_002232.2:n.*316G>T
|
|