ENST00000261609.13:c.11832G>A
MANE Select
|
ENSP00000261609.8:p.Trp3944Ter
|
|
ENST00000650509.1:c.3543G>A
|
ENSP00000496936.1:p.Trp1181Ter
|
|
ENST00000261609.11:c.11832G>A
|
ENSP00000261609.7:p.Trp3944Ter
|
|
NM_004667.5:c.11832G>A
|
NP_004658.3:p.Trp3944Ter
|
|
XM_005268276.3:c.11718G>A
|
XP_005268333.1:p.Trp3906Ter
|
|
XM_005268277.3:c.11718G>A
|
XP_005268334.1:p.Trp3906Ter
|
|
XM_006720726.2:c.11817G>A
|
XP_006720789.1:p.Trp3939Ter
|
|
XM_006720727.2:c.11574G>A
|
XP_006720790.1:p.Trp3858Ter
|
|
XM_011522131.1:c.11349G>A
|
XP_011520433.1:p.Trp3783Ter
|
|
XM_011522132.1:c.9348G>A
|
XP_011520434.1:p.Trp3116Ter
|
|
XM_011522133.1:c.8577G>A
|
XP_011520435.1:p.Trp2859Ter
|
|
XM_011522134.1:c.5949G>A
|
XP_011520436.1:p.Trp1983Ter
|
|
XM_005268276.5:c.11718G>A
|
XP_005268333.1:p.Trp3906Ter
|
|
XM_006720726.3:c.11817G>A
|
XP_006720789.1:p.Trp3939Ter
|
|
XM_006720727.3:c.11574G>A
|
XP_006720790.1:p.Trp3858Ter
|
|
XM_017022695.1:c.11718G>A
|
XP_016878184.1:p.Trp3906Ter
|
|
XM_017022696.1:c.11718G>A
|
XP_016878185.1:p.Trp3906Ter
|
|
XM_017022697.1:c.4998G>A
|
XP_016878186.1:p.Trp1666Ter
|
|
XM_017022698.1:c.4998G>A
|
XP_016878187.1:p.Trp1666Ter
|
|
NM_004667.6:c.11832G>A
MANE Select
|
NP_004658.3:p.Trp3944Ter
|
|