ENST00000267622.8:c.5160+151G>T
MANE Select
|
ENSP00000267622.4:n.5160+151G>T
|
|
ENST00000554357.5:c.4306+151G>T
|
|
|
ENST00000557017.1:c.408+151G>T
|
ENSP00000451607.1:n.408+151G>T
|
|
NM_004239.3:c.5160+151G>T
|
NP_004230.2:n.5160+151G>T
|
|
XM_005268214.2:c.3834+151G>T
|
XP_005268271.1:n.3834+151G>T
|
|
XM_005268215.2:c.2130+151G>T
|
XP_005268272.1:n.2130+151G>T
|
|
XM_006720321.2:c.5157+151G>T
|
XP_006720384.1:n.5157+151G>T
|
|
XR_943560.1:n.5615+151G>T
|
|
|
NM_001321851.1:c.5157+151G>T
|
NP_001308780.1:n.5157+151G>T
|
|
NM_004239.4:c.5160+151G>T
MANE Select
|
NP_004230.2:n.5160+151G>T
|
|
XM_017021787.2:c.4455+151G>T
|
XP_016877276.1:n.4455+151G>T
|
|
XM_017021788.2:c.3834+151G>T
|
XP_016877277.1:n.3834+151G>T
|
|
XR_001750598.2:n.5445+151G>T
|
|
|
XR_943560.2:n.5609+151G>T
|
|
|