ENST00000509700.2:c.671+692G>T
|
|
|
ENST00000636689.1:n.95-1794G>T
|
|
|
ENST00000637644.1:c.487+904G>T
|
ENSP00000490282.1:n.487+904G>T
|
|
ENST00000638728.1:c.*251G>T
|
ENSP00000492619.1:n.*251G>T
|
|
ENST00000638840.1:c.919+194G>T
|
|
|
ENST00000638868.1:c.*251G>T
|
ENSP00000491250.1:n.*251G>T
|
|
ENST00000639408.1:c.488-541G>T
|
ENSP00000491635.1:n.488-541G>T
|
|
ENST00000640017.1:c.670-541G>T
|
ENSP00000491337.1:n.670-541G>T
|
|
ENST00000640914.1:c.125-541G>T
|
|
|
ENST00000644903.1:c.*251G>T
MANE Select
|
ENSP00000495557.1:n.*251G>T
|
|
ENST00000368089.3:c.*251G>T
|
ENSP00000357068.3:n.*251G>T
|
|
ENST00000509700.1:n.463-541G>T
|
|
|
NM_002241.4:c.*251G>T
|
NP_002232.2:n.*251G>T
|
|
NM_002241.5:c.*251G>T
MANE Select
|
NP_002232.2:n.*251G>T
|
|