ENST00000266771.10:c.681G>T
MANE Select
|
ENSP00000266771.5:p.Ala227=
|
|
ENST00000266771.9:c.681G>T
|
ENSP00000266771.5:p.Ala227=
|
|
ENST00000366292.6:n.993G>T
|
|
|
ENST00000376740.8:c.260G>T
|
|
|
ENST00000376744.8:c.517G>T
|
|
|
ENST00000539703.1:n.331G>T
|
|
|
ENST00000614634.1:c.-162G>T
|
ENSP00000483143.1:n.-162G>T
|
|
NM_145648.3:c.681G>T
|
NP_663623.1:p.Ala227=
|
|
XM_011537895.1:c.831G>T
|
XP_011536197.1:p.Ala277=
|
|
XR_429081.2:n.704G>T
|
|
|
XR_944494.1:n.854G>T
|
|
|
XR_944495.1:n.854G>T
|
|
|
XR_944496.1:n.854G>T
|
|
|
XR_944497.1:n.854G>T
|
|
|
XM_017018791.1:c.831G>T
|
XP_016874280.1:p.Ala277=
|
|
XM_017018792.1:c.831G>T
|
XP_016874281.1:p.Ala277=
|
|
XM_017018793.1:c.681G>T
|
XP_016874282.1:p.Ala227=
|
|
XR_002957287.1:n.704G>T
|
|
|
XR_944496.2:n.854G>T
|
|
|
NM_145648.4:c.681G>T
MANE Select
|
NP_663623.1:p.Ala227=
|
|