ENST00000563236.6:c.2906_2907delinsAC
MANE Select
|
ENSP00000456149.2:p.Asp969=
|
|
ENST00000262502.5:c.2903_2904delinsAC
|
ENSP00000262502.5:p.Asp968=
|
|
ENST00000438926.6:c.2933_2934delinsAC
|
ENSP00000402152.2:p.Asp978=
|
|
ENST00000563236.5:c.2906_2907delinsAC
|
ENSP00000456149.1:p.Asp969=
|
|
ENST00000566786.5:c.2930_2931delinsAC
|
ENSP00000457552.1:p.Asp977=
|
|
ENST00000569002.1:n.337_338delinsAC
|
|
|
NM_000339.2:c.2933_2934delinsAC
|
NP_000330.2:p.Asp978=
|
|
NM_001126107.1:c.2930_2931delinsAC
|
NP_001119579.1:p.Asp977=
|
|
NM_001126108.1:c.2906_2907delinsAC
|
NP_001119580.1:p.Asp969=
|
|
XM_005256119.1:c.2903_2904delinsAC
|
XP_005256176.1:p.Asp968=
|
|
XM_005256119.2:c.2903_2904delinsAC
|
XP_005256176.1:p.Asp968=
|
|
NM_000339.3:c.2933_2934delinsAC
|
NP_000330.3:p.Asp978=
|
|
NM_001126107.2:c.2930_2931delinsAC
|
NP_001119579.2:p.Asp977=
|
|
NM_001126108.2:c.2906_2907delinsAC
MANE Select
|
NP_001119580.2:p.Asp969=
|
|