|
NM_001009944.3:c.9829C>G
MANE Select
|
NP_001009944.3:p.Arg3277Gly
|
|
ENST00000262304.9:c.9829C>G
MANE Select
|
ENSP00000262304.4:p.Arg3277Gly
|
|
NM_000296.3:c.9829C>G
|
NP_000287.3:p.Arg3277Gly
|
|
NM_000296.4:c.9829C>G
|
NP_000287.4:p.Arg3277Gly
|
|
NM_001009944.2:c.9829C>G
|
NP_001009944.2:p.Arg3277Gly
|
|
ENST00000262304.8:c.9829C>G
|
ENSP00000262304.4:p.Arg3277Gly
|
|
ENST00000415938.7:n.2908C>G
|
|
|
ENST00000423118.5:c.9829C>G
|
ENSP00000399501.1:p.Arg3277Gly
|
|
ENST00000469851.1:n.638C>G
|
|
|
ENST00000471603.6:n.1473C>G
|
|
|
ENST00000480227.5:n.1566C>G
|
|
|
ENST00000483731.5:n.3715C>G
|
|
|
ENST00000486339.6:n.3965C>G
|
|
|
ENST00000487932.5:c.4391C>G
|
ENSP00000457132.1:n.4391C>G
|
|
ENST00000496574.6:n.4065C>G
|
|
|
ENST00000562297.5:n.1562C>G
|
|
|
ENST00000566905.5:n.319C>G
|
|
|
ENST00000567946.1:c.1431C>G
|
|
|
ENST00000570193.5:n.273C>G
|
|
|
ENST00000570253.5:n.252C>G
|
|
|
XM_005255370.2:c.6784C>G
|
XP_005255427.1:p.Arg2262Gly
|
|
XM_005255370.3:c.6784C>G
|
XP_005255427.1:p.Arg2262Gly
|
|
XM_011522525.1:c.9907C>G
|
XP_011520827.1:p.Arg3303Gly
|
|
XM_011522526.1:c.9907C>G
|
XP_011520828.1:p.Arg3303Gly
|
|
XM_011522527.1:c.9889C>G
|
XP_011520829.1:p.Arg3297Gly
|
|
XM_011522528.1:c.9883C>G
|
XP_011520830.1:p.Arg3295Gly
|
|
XM_011522528.3:c.9883C>G
|
XP_011520830.1:p.Arg3295Gly
|
|
XM_011522529.1:c.9883C>G
|
XP_011520831.1:p.Arg3295Gly
|
|
XM_011522529.2:c.9883C>G
|
XP_011520831.1:p.Arg3295Gly
|
|
XM_011522530.1:c.9853C>G
|
XP_011520832.1:p.Arg3285Gly
|
|
XM_011522531.1:c.9835C>G
|
XP_011520833.1:p.Arg3279Gly
|
|
XM_011522532.1:c.9781C>G
|
XP_011520834.1:p.Arg3261Gly
|
|
XM_011522533.1:c.9700C>G
|
XP_011520835.1:p.Arg3234Gly
|
|
XM_011522534.1:c.9643C>G
|
XP_011520836.1:p.Arg3215Gly
|
|
XM_011522535.1:c.7729C>G
|
XP_011520837.1:p.Arg2577Gly
|
|
XM_011522536.1:c.9907C>G
|
XP_011520838.1:p.Arg3303Gly
|
|
XM_011522537.1:c.6907C>G
|
XP_011520839.1:p.Arg2303Gly
|
|
XM_011522537.2:c.6907C>G
|
XP_011520839.1:p.Arg2303Gly
|
|
XM_024450298.1:c.9949C>G
|
XP_024306066.1:p.Arg3317Gly
|
|
XM_024450299.1:c.9877C>G
|
XP_024306067.1:p.Arg3293Gly
|
|
XM_024450300.1:c.9739C>G
|
XP_024306068.1:p.Arg3247Gly
|
|
XM_024450301.1:c.7825C>G
|
XP_024306069.1:p.Arg2609Gly
|
|
XR_932867.1:n.9922C>G
|
|
|
XR_932868.1:n.9922C>G
|
|
|
XR_932869.1:n.9922C>G
|
|
|
XR_932870.1:n.9922C>G
|
|
