ENST00000261609.13:c.11935T=
MANE Select
|
ENSP00000261609.8:p.Cys3979=
|
|
ENST00000650509.1:c.3646T=
|
ENSP00000496936.1:p.Cys1216=
|
|
ENST00000261609.11:c.11935T=
|
ENSP00000261609.7:p.Cys3979=
|
|
NM_004667.5:c.11935T=
|
NP_004658.3:p.Cys3979=
|
|
XM_005268276.3:c.11821T=
|
XP_005268333.1:p.Cys3941=
|
|
XM_005268277.3:c.11821T=
|
XP_005268334.1:p.Cys3941=
|
|
XM_006720726.2:c.11920T=
|
XP_006720789.1:p.Cys3974=
|
|
XM_006720727.2:c.11677T=
|
XP_006720790.1:p.Cys3893=
|
|
XM_011522131.1:c.11452T=
|
XP_011520433.1:p.Cys3818=
|
|
XM_011522132.1:c.9451T=
|
XP_011520434.1:p.Cys3151=
|
|
XM_011522133.1:c.8680T=
|
XP_011520435.1:p.Cys2894=
|
|
XM_011522134.1:c.6052T=
|
XP_011520436.1:p.Cys2018=
|
|
XM_005268276.5:c.11821T=
|
XP_005268333.1:p.Cys3941=
|
|
XM_006720726.3:c.11920T=
|
XP_006720789.1:p.Cys3974=
|
|
XM_006720727.3:c.11677T=
|
XP_006720790.1:p.Cys3893=
|
|
XM_017022695.1:c.11821T=
|
XP_016878184.1:p.Cys3941=
|
|
XM_017022696.1:c.11821T=
|
XP_016878185.1:p.Cys3941=
|
|
XM_017022697.1:c.5101T=
|
XP_016878186.1:p.Cys1701=
|
|
XM_017022698.1:c.5101T=
|
XP_016878187.1:p.Cys1701=
|
|
NM_004667.6:c.11935T=
MANE Select
|
NP_004658.3:p.Cys3979=
|
|