ENST00000589419.2:n.990+62A>G
|
|
|
ENST00000650467.2:c.765+62A>G
|
ENSP00000496897.2:n.765+62A>G
|
|
ENST00000695903.1:c.*58A>G
|
ENSP00000512255.1:n.*58A>G
|
|
ENST00000695904.1:c.1100+62A>G
|
ENSP00000512259.1:n.1100+62A>G
|
|
ENST00000439986.9:c.987+62A>G
MANE Select
|
ENSP00000404464.2:n.987+62A>G
|
|
ENST00000589116.2:n.695+62A>G
|
|
|
ENST00000649564.1:c.987+62A>G
|
ENSP00000497183.1:n.987+62A>G
|
|
ENST00000650467.1:c.643+62A>G
|
|
|
ENST00000398179.3:c.777+62A>G
|
ENSP00000381241.3:n.777+62A>G
|
|
ENST00000439986.8:c.987+62A>G
|
ENSP00000404464.2:n.987+62A>G
|
|
ENST00000589116.1:n.695+62A>G
|
|
|
NM_133459.3:c.987+62A>G
|
NP_597716.1:n.987+62A>G
|
|
XM_005266648.2:c.987+62A>G
|
XP_005266705.1:n.987+62A>G
|
|
NM_133459.4:c.987+62A>G
MANE Select
|
NP_597716.1:n.987+62A>G
|
|
XM_017025556.1:c.1100+62A>G
|
XP_016881045.1:n.1100+62A>G
|
|
XM_017025557.1:c.1100+62A>G
|
XP_016881046.1:n.1100+62A>G
|
|
XM_017025558.1:c.1049A>G
|
XP_016881047.1:p.Glu350Gly
|
|
XM_024451091.1:c.987+62A>G
|
XP_024306859.1:n.987+62A>G
|
|
XR_001753142.1:n.2001A>G
|
|
|