ENST00000265104.5:c.8186G>A
MANE Select
|
ENSP00000265104.4:p.Cys2729Tyr
|
|
ENST00000681290.1:c.8141G>A
|
ENSP00000505288.1:p.Cys2714Tyr
|
|
ENST00000265104.4:c.8186G>A
|
ENSP00000265104.4:p.Cys2729Tyr
|
|
NM_001369.2:c.8186G>A
|
NP_001360.1:p.Cys2729Tyr
|
|
XM_005248262.2:c.8141G>A
|
XP_005248319.1:p.Cys2714Tyr
|
|
XM_011513990.1:c.8186G>A
|
XP_011512292.1:p.Cys2729Tyr
|
|
XR_925598.1:n.8393G>A
|
|
|
XM_005248262.3:c.8294G>A
|
XP_005248319.2:p.Cys2765Tyr
|
|
XM_017009177.1:c.8294G>A
|
XP_016864666.1:p.Cys2765Tyr
|
|
XM_017009178.1:c.7199G>A
|
XP_016864667.1:p.Cys2400Tyr
|
|
XM_017009179.2:c.7199G>A
|
XP_016864668.1:p.Cys2400Tyr
|
|
XM_017009180.1:c.8294G>A
|
XP_016864669.1:p.Cys2765Tyr
|
|
XM_017009181.1:c.8294G>A
|
XP_016864670.1:p.Cys2765Tyr
|
|
XM_017009182.1:c.8294G>A
|
XP_016864671.1:p.Cys2765Tyr
|
|
XM_017009183.1:c.8294G>A
|
XP_016864672.1:p.Cys2765Tyr
|
|
XM_017009184.1:c.8294G>A
|
XP_016864673.1:p.Cys2765Tyr
|
|
XM_017009185.1:c.3383G>A
|
XP_016864674.1:p.Cys1128Tyr
|
|
XM_017009186.1:c.2936G>A
|
XP_016864675.1:p.Cys979Tyr
|
|
XM_017009188.1:c.2273G>A
|
XP_016864677.1:p.Cys758Tyr
|
|
XM_024454388.1:c.7199G>A
|
XP_024310156.1:p.Cys2400Tyr
|
|
XM_024454389.1:c.6788G>A
|
XP_024310157.1:p.Cys2263Tyr
|
|
XR_001742034.1:n.8311G>A
|
|
|
XR_001742035.1:n.8311G>A
|
|
|
NM_001369.3:c.8186G>A
MANE Select
|
NP_001360.1:p.Cys2729Tyr
|
|