ENST00000416569.3:c.764+18269A>C
MANE Select
|
ENSP00000416707.2:n.764+18269A>C
|
|
ENST00000416569.2:c.764+18269A>C
|
ENSP00000416707.2:n.764+18269A>C
|
|
ENST00000529336.1:c.259+18269A>C
|
|
|
NM_173683.3:c.764+18269A>C
|
NP_775954.2:n.764+18269A>C
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|
XM_011543820.1:c.*31+12784A>C
|
XP_011542122.1:n.*31+12784A>C
|
|
XR_948899.1:n.937+12784A>C
|
|
|
NR_138152.1:n.922+12784A>C
|
|
|
NR_138153.1:n.791+18269A>C
|
|
|
NR_138154.1:n.791+18269A>C
|
|
|
XM_024447129.1:c.764+18269A>C
|
XP_024302897.1:n.764+18269A>C
|
|
XR_001745511.2:n.965+12784A>C
|
|
|
XR_948899.3:n.965+12784A>C
|
|
|
NM_173683.4:c.764+18269A>C
MANE Select
|
NP_775954.2:n.764+18269A>C
|
|
NR_138152.2:n.1389+12784A>C
|
|
|
NR_138153.2:n.1258+18269A>C
|
|
|
NR_138154.2:n.1258+18269A>C
|
|
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