ENST00000284885.8:c.1428+2T>G
MANE Select
|
ENSP00000284885.3:n.1428+2T>G
|
|
ENST00000284885.7:c.1428+2T>G
|
ENSP00000284885.3:n.1428+2T>G
|
|
NM_002772.2:c.1428+2T>G
|
NP_002763.2:n.1428+2T>G
|
|
XM_011529654.1:c.1563+2T>G
|
XP_011527956.1:n.1563+2T>G
|
|
XM_011529655.1:c.1563+2T>G
|
XP_011527957.1:n.1563+2T>G
|
|
XM_011529656.1:c.1563+2T>G
|
XP_011527958.1:n.1563+2T>G
|
|
XM_011529657.1:c.1518+2T>G
|
XP_011527959.1:n.1518+2T>G
|
|
XM_011529658.1:c.1482+2T>G
|
XP_011527960.1:n.1482+2T>G
|
|
XM_011529659.1:c.1473+2T>G
|
XP_011527961.1:n.1473+2T>G
|
|
XM_011529654.2:c.1563+2T>G
|
XP_011527956.1:n.1563+2T>G
|
|
XM_011529656.2:c.1563+2T>G
|
XP_011527958.1:n.1563+2T>G
|
|
XM_011529657.2:c.1518+2T>G
|
XP_011527959.1:n.1518+2T>G
|
|
XM_011529658.2:c.1482+2T>G
|
XP_011527960.1:n.1482+2T>G
|
|
NM_002772.3:c.1428+2T>G
MANE Select
|
NP_002763.3:n.1428+2T>G
|
|