ENST00000278829.7:c.213+3378_213+3390delinsACTCATTGATTCT
MANE Select
|
ENSP00000278829.2:n.213+3378_213+3390deli...
|
|
ENST00000278829.6:c.213+3378_213+3390delinsACTCATTGATTCT
|
ENSP00000278829.2:n.213+3378_213+3390deli...
|
|
ENST00000414624.6:n.286+3378_286+3390delinsACTCATTGATTCT
|
|
|
ENST00000525588.5:c.213+3378_213+3390delinsACTCATTGATTCT
|
ENSP00000432206.1:n.213+3378_213+3390deli...
|
|
ENST00000527697.5:c.-160+4068_-160+4080delinsACTCATTGATTCT
|
ENSP00000431533.1:n.-160+4068_-160+4080de...
|
|
NM_021727.4:c.213+3378_213+3390delinsACTCATTGATTCT
|
NP_068373.1:n.213+3378_213+3390delinsACTC...
|
|
XM_011545023.1:c.213+3378_213+3390delinsACTCATTGATTCT
|
XP_011543325.1:n.213+3378_213+3390delinsA...
|
|
XM_011545023.2:c.213+3378_213+3390delinsACTCATTGATTCT
|
XP_011543325.1:n.213+3378_213+3390delinsA...
|
|
XM_017017723.1:c.351+4068_351+4080delinsACTCATTGATTCT
|
XP_016873212.1:n.351+4068_351+4080delinsA...
|
|
XM_017017724.1:c.351+4068_351+4080delinsACTCATTGATTCT
|
XP_016873213.1:n.351+4068_351+4080delinsA...
|
|
XR_001747866.1:n.366+4068_366+4080delinsACTCATTGATTCT
|
|
|
XR_001747867.1:n.366+4068_366+4080delinsACTCATTGATTCT
|
|
|
XR_001747868.1:n.377+3378_377+3390delinsACTCATTGATTCT
|
|
|
XR_001747869.1:n.377+3378_377+3390delinsACTCATTGATTCT
|
|
|
NM_021727.5:c.213+3378_213+3390delinsACTCATTGATTCT
MANE Select
|
NP_068373.1:n.213+3378_213+3390delinsACTC...
|
|