ENST00000265104.5:c.9410G=
MANE Select
|
ENSP00000265104.4:p.Cys3137=
|
|
ENST00000681290.1:c.9365G=
|
ENSP00000505288.1:p.Cys3122=
|
|
ENST00000265104.4:c.9410G=
|
ENSP00000265104.4:p.Cys3137=
|
|
ENST00000504001.3:n.122G=
|
|
|
NM_001369.2:c.9410G=
|
NP_001360.1:p.Cys3137=
|
|
XM_005248262.2:c.9365G=
|
XP_005248319.1:p.Cys3122=
|
|
XM_005248262.3:c.9518G=
|
XP_005248319.2:p.Cys3173=
|
|
XM_017009177.1:c.9518G=
|
XP_016864666.1:p.Cys3173=
|
|
XM_017009178.1:c.8423G=
|
XP_016864667.1:p.Cys2808=
|
|
XM_017009179.2:c.8423G=
|
XP_016864668.1:p.Cys2808=
|
|
XM_017009180.1:c.9518G=
|
XP_016864669.1:p.Cys3173=
|
|
XM_017009181.1:c.9518G=
|
XP_016864670.1:p.Cys3173=
|
|
XM_017009182.1:c.9518G=
|
XP_016864671.1:p.Cys3173=
|
|
XM_017009183.1:c.9518G=
|
XP_016864672.1:p.Cys3173=
|
|
XM_017009185.1:c.4607G=
|
XP_016864674.1:p.Cys1536=
|
|
XM_017009186.1:c.4160G=
|
XP_016864675.1:p.Cys1387=
|
|
XM_017009188.1:c.3497G=
|
XP_016864677.1:p.Cys1166=
|
|
XM_024454388.1:c.8423G=
|
XP_024310156.1:p.Cys2808=
|
|
XM_024454389.1:c.8012G=
|
XP_024310157.1:p.Cys2671=
|
|
NM_001369.3:c.9410G=
MANE Select
|
NP_001360.1:p.Cys3137=
|
|