ENST00000710270.1:c.3129A>T
|
ENSP00000518163.1:p.Ala1043=
|
|
ENST00000392723.6:c.2922A>T
|
ENSP00000376484.1:p.Ala974=
|
|
ENST00000439756.2:c.3081A>T
|
ENSP00000390156.2:p.Ala1027=
|
|
ENST00000703168.1:c.3102A>T
|
ENSP00000515214.1:p.Ala1034=
|
|
ENST00000271715.7:c.3081A>T
MANE Select
|
ENSP00000271715.2:p.Ala1027=
|
|
ENST00000271715.6:c.3081A>T
|
ENSP00000271715.2:p.Ala1027=
|
|
ENST00000358476.7:n.3229A>T
|
|
|
ENST00000368863.6:c.2796A>T
|
ENSP00000357856.2:p.Ala932=
|
|
ENST00000392723.5:c.2922A>T
|
ENSP00000376484.1:p.Ala974=
|
|
ENST00000409503.5:c.3054A>T
|
ENSP00000386836.1:p.Ala1018=
|
|
ENST00000491586.5:c.2949A>T
|
ENSP00000418408.1:p.Ala983=
|
|
ENST00000531094.5:c.2895A>T
|
ENSP00000431259.1:p.Ala965=
|
|
NM_001194937.1:c.3054A>T
|
NP_001181866.1:p.Ala1018=
|
|
NM_001194938.1:c.2895A>T
|
NP_001181867.1:p.Ala965=
|
|
NM_015100.3:c.3081A>T
|
NP_055915.2:p.Ala1027=
|
|
NM_145796.3:c.2796A>T
|
NP_665739.3:p.Ala932=
|
|
NM_207171.2:c.2922A>T
|
NP_997054.1:p.Ala974=
|
|
XM_005244999.1:c.3081A>T
|
XP_005245056.1:p.Ala1027=
|
|
XM_005245000.3:c.3081A>T
|
XP_005245057.1:p.Ala1027=
|
|
XM_005245001.1:c.3081A>T
|
XP_005245058.1:p.Ala1027=
|
|
XM_005245005.1:c.2922A>T
|
XP_005245062.1:p.Ala974=
|
|
XM_005245006.3:c.2922A>T
|
XP_005245063.1:p.Ala974=
|
|
XM_011509330.1:c.2973A>T
|
XP_011507632.1:p.Ala991=
|
|
XM_011509331.1:c.2724A>T
|
XP_011507633.1:p.Ala908=
|
|
XM_005244999.3:c.3081A>T
|
XP_005245056.1:p.Ala1027=
|
|
XM_005245000.4:c.3081A>T
|
XP_005245057.1:p.Ala1027=
|
|
XM_005245001.2:c.3081A>T
|
XP_005245058.1:p.Ala1027=
|
|
XM_005245005.2:c.2922A>T
|
XP_005245062.1:p.Ala974=
|
|
XM_005245006.5:c.2922A>T
|
XP_005245063.1:p.Ala974=
|
|
XM_017000744.1:c.3102A>T
|
XP_016856233.1:p.Ala1034=
|
|
XM_017000745.2:c.3054A>T
|
XP_016856234.1:p.Ala1018=
|
|
XM_017000746.1:c.3054A>T
|
XP_016856235.1:p.Ala1018=
|
|
XM_017000748.1:c.2922A>T
|
XP_016856237.1:p.Ala974=
|
|
XM_017000749.1:c.2922A>T
|
XP_016856238.1:p.Ala974=
|
|
XM_024454305.1:c.2955A>T
|
XP_024310073.1:p.Ala985=
|
|
XM_024454306.1:c.1881A>T
|
XP_024310074.1:p.Ala627=
|
|
XR_002959801.1:n.2936A>T
|
|
|
NM_015100.4:c.3081A>T
MANE Select
|
NP_055915.2:p.Ala1027=
|
|
NM_001194937.2:c.3054A>T
|
NP_001181866.1:p.Ala1018=
|
|
NM_001194938.2:c.2895A>T
|
NP_001181867.1:p.Ala965=
|
|
NM_145796.4:c.2796A>T
|
NP_665739.3:p.Ala932=
|
|