ENST00000248633.9:c.2210T=
MANE Select
|
ENSP00000248633.4:p.Ile737=
|
|
ENST00000248633.8:c.2210T=
|
ENSP00000248633.4:p.Ile737=
|
|
ENST00000428214.5:c.2039T=
|
ENSP00000394413.1:p.Ile680=
|
|
ENST00000438045.5:c.1244T=
|
ENSP00000410438.1:p.Ile415=
|
|
ENST00000484913.5:n.2249T=
|
|
|
ENST00000496092.1:n.8T=
|
|
|
ENST00000496420.5:n.1886T=
|
|
|
NM_000466.2:c.2210T=
|
NP_000457.1:p.Ile737=
|
|
NM_001282677.1:c.2039T=
|
NP_001269606.1:p.Ile680=
|
|
NM_001282678.1:c.1586T=
|
NP_001269607.1:p.Ile529=
|
|
XM_005250433.3:c.461T=
|
XP_005250490.1:p.Ile154=
|
|
XR_242246.3:n.2306T=
|
|
|
XM_017012319.2:c.461T=
|
XP_016867808.1:p.Ile154=
|
|
XR_001744808.2:n.1237T=
|
|
|
XR_242246.5:n.2257T=
|
|
|
NM_000466.3:c.2210T=
MANE Select
|
NP_000457.1:p.Ile737=
|
|
NM_001282677.2:c.2039T=
|
NP_001269606.1:p.Ile680=
|
|
NM_001282678.2:c.1586T=
|
NP_001269607.1:p.Ile529=
|
|