ENST00000261609.13:c.11938G>T
MANE Select
|
ENSP00000261609.8:p.Glu3980Ter
|
|
ENST00000650509.1:c.3649G>T
|
ENSP00000496936.1:p.Glu1217Ter
|
|
ENST00000261609.11:c.11938G>T
|
ENSP00000261609.7:p.Glu3980Ter
|
|
NM_004667.5:c.11938G>T
|
NP_004658.3:p.Glu3980Ter
|
|
XM_005268276.3:c.11824G>T
|
XP_005268333.1:p.Glu3942Ter
|
|
XM_005268277.3:c.11824G>T
|
XP_005268334.1:p.Glu3942Ter
|
|
XM_006720726.2:c.11923G>T
|
XP_006720789.1:p.Glu3975Ter
|
|
XM_006720727.2:c.11680G>T
|
XP_006720790.1:p.Glu3894Ter
|
|
XM_011522131.1:c.11455G>T
|
XP_011520433.1:p.Glu3819Ter
|
|
XM_011522132.1:c.9454G>T
|
XP_011520434.1:p.Glu3152Ter
|
|
XM_011522133.1:c.8683G>T
|
XP_011520435.1:p.Glu2895Ter
|
|
XM_011522134.1:c.6055G>T
|
XP_011520436.1:p.Glu2019Ter
|
|
XM_005268276.5:c.11824G>T
|
XP_005268333.1:p.Glu3942Ter
|
|
XM_006720726.3:c.11923G>T
|
XP_006720789.1:p.Glu3975Ter
|
|
XM_006720727.3:c.11680G>T
|
XP_006720790.1:p.Glu3894Ter
|
|
XM_017022695.1:c.11824G>T
|
XP_016878184.1:p.Glu3942Ter
|
|
XM_017022696.1:c.11824G>T
|
XP_016878185.1:p.Glu3942Ter
|
|
XM_017022697.1:c.5104G>T
|
XP_016878186.1:p.Glu1702Ter
|
|
XM_017022698.1:c.5104G>T
|
XP_016878187.1:p.Glu1702Ter
|
|
NM_004667.6:c.11938G>T
MANE Select
|
NP_004658.3:p.Glu3980Ter
|
|