ENST00000261609.13:c.11980G>T
MANE Select
|
ENSP00000261609.8:p.Glu3994Ter
|
|
ENST00000650509.1:c.3691G>T
|
ENSP00000496936.1:p.Glu1231Ter
|
|
ENST00000261609.11:c.11980G>T
|
ENSP00000261609.7:p.Glu3994Ter
|
|
NM_004667.5:c.11980G>T
|
NP_004658.3:p.Glu3994Ter
|
|
XM_005268276.3:c.11866G>T
|
XP_005268333.1:p.Glu3956Ter
|
|
XM_005268277.3:c.11866G>T
|
XP_005268334.1:p.Glu3956Ter
|
|
XM_006720726.2:c.11965G>T
|
XP_006720789.1:p.Glu3989Ter
|
|
XM_006720727.2:c.11722G>T
|
XP_006720790.1:p.Glu3908Ter
|
|
XM_011522131.1:c.11497G>T
|
XP_011520433.1:p.Glu3833Ter
|
|
XM_011522132.1:c.9496G>T
|
XP_011520434.1:p.Glu3166Ter
|
|
XM_011522133.1:c.8725G>T
|
XP_011520435.1:p.Glu2909Ter
|
|
XM_011522134.1:c.6097G>T
|
XP_011520436.1:p.Glu2033Ter
|
|
XM_005268276.5:c.11866G>T
|
XP_005268333.1:p.Glu3956Ter
|
|
XM_006720726.3:c.11965G>T
|
XP_006720789.1:p.Glu3989Ter
|
|
XM_006720727.3:c.11722G>T
|
XP_006720790.1:p.Glu3908Ter
|
|
XM_017022695.1:c.11866G>T
|
XP_016878184.1:p.Glu3956Ter
|
|
XM_017022696.1:c.11866G>T
|
XP_016878185.1:p.Glu3956Ter
|
|
XM_017022697.1:c.5146G>T
|
XP_016878186.1:p.Glu1716Ter
|
|
XM_017022698.1:c.5146G>T
|
XP_016878187.1:p.Glu1716Ter
|
|
NM_004667.6:c.11980G>T
MANE Select
|
NP_004658.3:p.Glu3994Ter
|
|