|
NM_001308120.2:c.4150C>T
MANE Select
|
NP_001295049.1:p.Gln1384Ter
|
|
ENST00000361462.7:c.4150C>T
MANE Select
|
ENSP00000354917.2:p.Gln1384Ter
|
|
NM_001308120.1:c.4150C>T
|
NP_001295049.1:p.Gln1384Ter
|
|
NM_015091.2:c.4150C>T
|
NP_055906.2:p.Gln1384Ter
|
|
NM_015091.3:c.4150C>T
|
NP_055906.2:p.Gln1384Ter
|
|
NM_015091.4:c.4150C>T
|
NP_055906.2:p.Gln1384Ter
|
|
NR_131765.1:n.4213C>T
|
|
|
NR_131765.2:n.4213C>T
|
|
|
ENST00000361462.6:c.4150C>T
|
ENSP00000354917.2:p.Gln1384Ter
|
|
ENST00000361577.7:c.4150C>T
|
ENSP00000355045.3:p.Gln1384Ter
|
|
ENST00000557423.5:c.*993C>T
|
ENSP00000451829.1:n.*993C>T
|
|
XM_011536571.1:c.4150C>T
|
XP_011534873.1:p.Gln1384Ter
|
|
XM_011536572.1:c.4150C>T
|
XP_011534874.1:p.Gln1384Ter
|
|
XM_017021098.1:c.4060C>T
|
XP_016876587.1:p.Gln1354Ter
|
|
XM_017021099.1:c.3844C>T
|
XP_016876588.1:p.Gln1282Ter
|
|
XR_001750194.1:n.4353C>T
|
|
|
XR_001750195.1:n.4120C>T
|
|