ENST00000330342.8:c.1326+127T>G
MANE Select
|
ENSP00000332247.2:n.1326+127T>G
|
|
ENST00000540368.6:n.1357+127T>G
|
|
|
ENST00000674794.1:c.1414+127T>G
|
|
|
ENST00000675260.1:n.601+127T>G
|
|
|
ENST00000675344.1:c.*347+127T>G
|
ENSP00000501953.1:n.*347+127T>G
|
|
ENST00000330342.7:c.1326+127T>G
|
ENSP00000332247.2:n.1326+127T>G
|
|
ENST00000504192.2:c.936+127T>G
|
ENSP00000443441.1:n.936+127T>G
|
|
ENST00000536426.1:n.343+127T>G
|
|
|
ENST00000545059.5:n.3962+127T>G
|
|
|
NM_012463.3:c.1326+127T>G
|
NP_036595.2:n.1326+127T>G
|
|
XM_005253563.1:c.1326+127T>G
|
XP_005253620.1:n.1326+127T>G
|
|
XM_006719317.2:c.813+127T>G
|
XP_006719380.1:n.813+127T>G
|
|
XM_006719318.2:c.504+127T>G
|
XP_006719381.1:n.504+127T>G
|
|
XR_429088.1:n.1489+127T>G
|
|
|
XM_024448910.1:c.1326+127T>G
|
XP_024304678.1:n.1326+127T>G
|
|
XM_024448911.1:c.813+127T>G
|
XP_024304679.1:n.813+127T>G
|
|
XM_024448912.1:c.504+127T>G
|
XP_024304680.1:n.504+127T>G
|
|
NM_012463.4:c.1326+127T>G
MANE Select
|
NP_036595.2:n.1326+127T>G
|
|