ENST00000563236.6:c.2884A=
MANE Select
|
ENSP00000456149.2:p.Ile962=
|
|
ENST00000262502.5:c.2881A=
|
ENSP00000262502.5:p.Ile961=
|
|
ENST00000438926.6:c.2911A=
|
ENSP00000402152.2:p.Ile971=
|
|
ENST00000563236.5:c.2884A=
|
ENSP00000456149.1:p.Ile962=
|
|
ENST00000566786.5:c.2908A=
|
ENSP00000457552.1:p.Ile970=
|
|
ENST00000569002.1:n.315A=
|
|
|
NM_000339.2:c.2911A=
|
NP_000330.2:p.Ile971=
|
|
NM_001126107.1:c.2908A=
|
NP_001119579.1:p.Ile970=
|
|
NM_001126108.1:c.2884A=
|
NP_001119580.1:p.Ile962=
|
|
XM_005256119.1:c.2881A=
|
XP_005256176.1:p.Ile961=
|
|
XM_005256119.2:c.2881A=
|
XP_005256176.1:p.Ile961=
|
|
NM_000339.3:c.2911A=
|
NP_000330.3:p.Ile971=
|
|
NM_001126107.2:c.2908A=
|
NP_001119579.2:p.Ile970=
|
|
NM_001126108.2:c.2884A=
MANE Select
|
NP_001119580.2:p.Ile962=
|
|