ENST00000284031.13:c.303+30949T>A
MANE Select
|
ENSP00000284031.8:n.303+30949T>A
|
|
ENST00000426972.8:c.-7+62372T>A
|
ENSP00000411189.4:n.-7+62372T>A
|
|
ENST00000284031.12:c.303+30949T>A
|
ENSP00000284031.8:n.303+30949T>A
|
|
ENST00000426972.7:c.-7+62372T>A
|
ENSP00000411189.4:n.-7+62372T>A
|
|
ENST00000483110.5:n.383+62372T>A
|
|
|
ENST00000535924.6:c.-7+62372T>A
|
ENSP00000439045.1:n.-7+62372T>A
|
|
ENST00000539042.3:c.303+30949T>A
|
ENSP00000438604.1:n.303+30949T>A
|
|
NM_001134445.1:c.-7+62372T>A
|
NP_001127917.1:n.-7+62372T>A
|
|
NM_012137.3:c.303+30949T>A
|
NP_036269.1:n.303+30949T>A
|
|
XM_005270707.2:c.19-74947T>A
|
XP_005270764.1:n.19-74947T>A
|
|
XM_005270709.2:c.-7+62372T>A
|
XP_005270766.1:n.-7+62372T>A
|
|
XM_011541158.1:c.-87+62372T>A
|
XP_011539460.1:n.-87+62372T>A
|
|
XM_017000889.1:c.24+30702T>A
|
XP_016856378.1:n.24+30702T>A
|
|
XM_024446130.1:c.-7+62372T>A
|
XP_024301898.1:n.-7+62372T>A
|
|
NM_012137.4:c.303+30949T>A
MANE Select
|
NP_036269.1:n.303+30949T>A
|
|
NM_001134445.2:c.-7+62372T>A
|
NP_001127917.1:n.-7+62372T>A
|
|