ENST00000265104.5:c.10922T>A
MANE Select
|
ENSP00000265104.4:p.Leu3641His
|
|
ENST00000681290.1:c.10877T>A
|
ENSP00000505288.1:p.Leu3626His
|
|
ENST00000265104.4:c.10922T>A
|
ENSP00000265104.4:p.Leu3641His
|
|
NM_001369.2:c.10922T>A
|
NP_001360.1:p.Leu3641His
|
|
XM_005248262.2:c.10877T>A
|
XP_005248319.1:p.Leu3626His
|
|
XM_005248262.3:c.11030T>A
|
XP_005248319.2:p.Leu3677His
|
|
XM_017009177.1:c.11030T>A
|
XP_016864666.1:p.Leu3677His
|
|
XM_017009178.1:c.9935T>A
|
XP_016864667.1:p.Leu3312His
|
|
XM_017009179.2:c.9935T>A
|
XP_016864668.1:p.Leu3312His
|
|
XM_017009180.1:c.11030T>A
|
XP_016864669.1:p.Leu3677His
|
|
XM_017009181.1:c.11030T>A
|
XP_016864670.1:p.Leu3677His
|
|
XM_017009182.1:c.11030T>A
|
XP_016864671.1:p.Leu3677His
|
|
XM_017009185.1:c.6119T>A
|
XP_016864674.1:p.Leu2040His
|
|
XM_017009186.1:c.5672T>A
|
XP_016864675.1:p.Leu1891His
|
|
XM_017009188.1:c.5009T>A
|
XP_016864677.1:p.Leu1670His
|
|
XM_024454388.1:c.9935T>A
|
XP_024310156.1:p.Leu3312His
|
|
XM_024454389.1:c.9524T>A
|
XP_024310157.1:p.Leu3175His
|
|
NM_001369.3:c.10922T>A
MANE Select
|
NP_001360.1:p.Leu3641His
|
|