ENST00000248633.9:c.2086A=
MANE Select
|
ENSP00000248633.4:p.Ile696=
|
|
ENST00000248633.8:c.2086A=
|
ENSP00000248633.4:p.Ile696=
|
|
ENST00000428214.5:c.1915A=
|
ENSP00000394413.1:p.Ile639=
|
|
ENST00000438045.5:c.1120A=
|
ENSP00000410438.1:p.Ile374=
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|
ENST00000484913.5:n.2125A=
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|
|
ENST00000496420.5:n.1762A=
|
|
|
NM_000466.2:c.2086A=
|
NP_000457.1:p.Ile696=
|
|
NM_001282677.1:c.1915A=
|
NP_001269606.1:p.Ile639=
|
|
NM_001282678.1:c.1462A=
|
NP_001269607.1:p.Ile488=
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|
XM_005250433.3:c.337A=
|
XP_005250490.1:p.Ile113=
|
|
XR_242246.3:n.2182A=
|
|
|
XM_017012319.2:c.337A=
|
XP_016867808.1:p.Ile113=
|
|
XR_001744808.2:n.1113A=
|
|
|
XR_242246.5:n.2133A=
|
|
|
NM_000466.3:c.2086A=
MANE Select
|
NP_000457.1:p.Ile696=
|
|
NM_001282677.2:c.1915A=
|
NP_001269606.1:p.Ile639=
|
|
NM_001282678.2:c.1462A=
|
NP_001269607.1:p.Ile488=
|
|