ENST00000261609.13:c.11936G>A
MANE Select
|
ENSP00000261609.8:p.Cys3979Tyr
|
|
ENST00000650509.1:c.3647G>A
|
ENSP00000496936.1:p.Cys1216Tyr
|
|
ENST00000261609.11:c.11936G>A
|
ENSP00000261609.7:p.Cys3979Tyr
|
|
NM_004667.5:c.11936G>A
|
NP_004658.3:p.Cys3979Tyr
|
|
XM_005268276.3:c.11822G>A
|
XP_005268333.1:p.Cys3941Tyr
|
|
XM_005268277.3:c.11822G>A
|
XP_005268334.1:p.Cys3941Tyr
|
|
XM_006720726.2:c.11921G>A
|
XP_006720789.1:p.Cys3974Tyr
|
|
XM_006720727.2:c.11678G>A
|
XP_006720790.1:p.Cys3893Tyr
|
|
XM_011522131.1:c.11453G>A
|
XP_011520433.1:p.Cys3818Tyr
|
|
XM_011522132.1:c.9452G>A
|
XP_011520434.1:p.Cys3151Tyr
|
|
XM_011522133.1:c.8681G>A
|
XP_011520435.1:p.Cys2894Tyr
|
|
XM_011522134.1:c.6053G>A
|
XP_011520436.1:p.Cys2018Tyr
|
|
XM_005268276.5:c.11822G>A
|
XP_005268333.1:p.Cys3941Tyr
|
|
XM_006720726.3:c.11921G>A
|
XP_006720789.1:p.Cys3974Tyr
|
|
XM_006720727.3:c.11678G>A
|
XP_006720790.1:p.Cys3893Tyr
|
|
XM_017022695.1:c.11822G>A
|
XP_016878184.1:p.Cys3941Tyr
|
|
XM_017022696.1:c.11822G>A
|
XP_016878185.1:p.Cys3941Tyr
|
|
XM_017022697.1:c.5102G>A
|
XP_016878186.1:p.Cys1701Tyr
|
|
XM_017022698.1:c.5102G>A
|
XP_016878187.1:p.Cys1701Tyr
|
|
NM_004667.6:c.11936G>A
MANE Select
|
NP_004658.3:p.Cys3979Tyr
|
|