ENST00000248846.10:c.3606_3608delinsGTC
MANE Select
|
ENSP00000248846.5:p.Val1202=
|
|
ENST00000248846.9:c.3606_3608delinsGTC
|
ENSP00000248846.5:p.Val1202=
|
|
ENST00000439308.6:c.3606_3608delinsGTC
|
ENSP00000397387.2:p.Val1202=
|
|
ENST00000491449.5:n.1913_1915delinsGTC
|
|
|
ENST00000498611.5:n.3617+522_3617+524delinsGTC
|
|
|
NM_020461.3:c.3606_3608delinsGTC
|
NP_065194.2:p.Val1202=
|
|
XR_938347.1:n.4171_4173delinsGTC
|
|
|
XR_938348.1:n.3050-738_3050-736delinsGTC
|
|
|
XR_001755343.2:n.4175_4177delinsGTC
|
|
|
XR_001755344.2:n.4175_4177delinsGTC
|
|
|
XR_002958720.1:n.3054-738_3054-736delinsGTC
|
|
|
XR_938347.2:n.4175_4177delinsGTC
|
|
|
NM_020461.4:c.3606_3608delinsGTC
MANE Select
|
NP_065194.3:p.Val1202=
|
|