ENST00000265104.5:c.11520T>C
MANE Select
|
ENSP00000265104.4:p.Tyr3840=
|
|
ENST00000681290.1:c.11475T>C
|
ENSP00000505288.1:p.Tyr3825=
|
|
ENST00000265104.4:c.11520T>C
|
ENSP00000265104.4:p.Tyr3840=
|
|
NM_001369.2:c.11520T>C
|
NP_001360.1:p.Tyr3840=
|
|
XM_005248262.2:c.11475T>C
|
XP_005248319.1:p.Tyr3825=
|
|
XM_005248262.3:c.11628T>C
|
XP_005248319.2:p.Tyr3876=
|
|
XM_017009177.1:c.11628T>C
|
XP_016864666.1:p.Tyr3876=
|
|
XM_017009178.1:c.10533T>C
|
XP_016864667.1:p.Tyr3511=
|
|
XM_017009179.2:c.10533T>C
|
XP_016864668.1:p.Tyr3511=
|
|
XM_017009180.1:c.11628T>C
|
XP_016864669.1:p.Tyr3876=
|
|
XM_017009181.1:c.11628T>C
|
XP_016864670.1:p.Tyr3876=
|
|
XM_017009182.1:c.11384T>C
|
XP_016864671.1:p.Ile3795Thr
|
|
XM_017009185.1:c.6717T>C
|
XP_016864674.1:p.Tyr2239=
|
|
XM_017009186.1:c.6270T>C
|
XP_016864675.1:p.Tyr2090=
|
|
XM_017009188.1:c.5607T>C
|
XP_016864677.1:p.Tyr1869=
|
|
XM_024454388.1:c.10533T>C
|
XP_024310156.1:p.Tyr3511=
|
|
XM_024454389.1:c.10122T>C
|
XP_024310157.1:p.Tyr3374=
|
|
NM_001369.3:c.11520T>C
MANE Select
|
NP_001360.1:p.Tyr3840=
|
|