ENST00000261609.13:c.11788G>T
MANE Select
|
ENSP00000261609.8:p.Asp3930Tyr
|
|
ENST00000650509.1:c.3499G>T
|
ENSP00000496936.1:p.Asp1167Tyr
|
|
ENST00000261609.11:c.11788G>T
|
ENSP00000261609.7:p.Asp3930Tyr
|
|
ENST00000564519.1:n.303G>T
|
|
|
NM_004667.5:c.11788G>T
|
NP_004658.3:p.Asp3930Tyr
|
|
XM_005268276.3:c.11674G>T
|
XP_005268333.1:p.Asp3892Tyr
|
|
XM_005268277.3:c.11674G>T
|
XP_005268334.1:p.Asp3892Tyr
|
|
XM_006720726.2:c.11773G>T
|
XP_006720789.1:p.Asp3925Tyr
|
|
XM_006720727.2:c.11530G>T
|
XP_006720790.1:p.Asp3844Tyr
|
|
XM_011522131.1:c.11305G>T
|
XP_011520433.1:p.Asp3769Tyr
|
|
XM_011522132.1:c.9304G>T
|
XP_011520434.1:p.Asp3102Tyr
|
|
XM_011522133.1:c.8533G>T
|
XP_011520435.1:p.Asp2845Tyr
|
|
XM_011522134.1:c.5905G>T
|
XP_011520436.1:p.Asp1969Tyr
|
|
XM_005268276.5:c.11674G>T
|
XP_005268333.1:p.Asp3892Tyr
|
|
XM_006720726.3:c.11773G>T
|
XP_006720789.1:p.Asp3925Tyr
|
|
XM_006720727.3:c.11530G>T
|
XP_006720790.1:p.Asp3844Tyr
|
|
XM_017022695.1:c.11674G>T
|
XP_016878184.1:p.Asp3892Tyr
|
|
XM_017022696.1:c.11674G>T
|
XP_016878185.1:p.Asp3892Tyr
|
|
XM_017022697.1:c.4954G>T
|
XP_016878186.1:p.Asp1652Tyr
|
|
XM_017022698.1:c.4954G>T
|
XP_016878187.1:p.Asp1652Tyr
|
|
NM_004667.6:c.11788G>T
MANE Select
|
NP_004658.3:p.Asp3930Tyr
|
|