ENST00000278829.7:c.213+3743A>G
MANE Select
|
ENSP00000278829.2:n.213+3743A>G
|
|
ENST00000278829.6:c.213+3743A>G
|
ENSP00000278829.2:n.213+3743A>G
|
|
ENST00000414624.6:n.286+3743A>G
|
|
|
ENST00000525588.5:c.213+3743A>G
|
ENSP00000432206.1:n.213+3743A>G
|
|
ENST00000527697.5:c.-160+4433A>G
|
ENSP00000431533.1:n.-160+4433A>G
|
|
NM_021727.4:c.213+3743A>G
|
NP_068373.1:n.213+3743A>G
|
|
XM_011545023.1:c.213+3743A>G
|
XP_011543325.1:n.213+3743A>G
|
|
XM_011545023.2:c.213+3743A>G
|
XP_011543325.1:n.213+3743A>G
|
|
XM_017017723.1:c.351+4433A>G
|
XP_016873212.1:n.351+4433A>G
|
|
XM_017017724.1:c.351+4433A>G
|
XP_016873213.1:n.351+4433A>G
|
|
XR_001747866.1:n.366+4433A>G
|
|
|
XR_001747867.1:n.366+4433A>G
|
|
|
XR_001747868.1:n.377+3743A>G
|
|
|
XR_001747869.1:n.377+3743A>G
|
|
|
NM_021727.5:c.213+3743A>G
MANE Select
|
NP_068373.1:n.213+3743A>G
|
|