ENST00000248633.9:c.2209A>G
MANE Select
|
ENSP00000248633.4:p.Ile737Val
|
|
ENST00000248633.8:c.2209A>G
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ENSP00000248633.4:p.Ile737Val
|
|
ENST00000428214.5:c.2038A>G
|
ENSP00000394413.1:p.Ile680Val
|
|
ENST00000438045.5:c.1243A>G
|
ENSP00000410438.1:p.Ile415Val
|
|
ENST00000484913.5:n.2248A>G
|
|
|
ENST00000496092.1:n.7A>G
|
|
|
ENST00000496420.5:n.1885A>G
|
|
|
NM_000466.2:c.2209A>G
|
NP_000457.1:p.Ile737Val
|
|
NM_001282677.1:c.2038A>G
|
NP_001269606.1:p.Ile680Val
|
|
NM_001282678.1:c.1585A>G
|
NP_001269607.1:p.Ile529Val
|
|
XM_005250433.3:c.460A>G
|
XP_005250490.1:p.Ile154Val
|
|
XR_242246.3:n.2305A>G
|
|
|
XM_017012319.2:c.460A>G
|
XP_016867808.1:p.Ile154Val
|
|
XR_001744808.2:n.1236A>G
|
|
|
XR_242246.5:n.2256A>G
|
|
|
NM_000466.3:c.2209A>G
MANE Select
|
NP_000457.1:p.Ile737Val
|
|
NM_001282677.2:c.2038A>G
|
NP_001269606.1:p.Ile680Val
|
|
NM_001282678.2:c.1585A>G
|
NP_001269607.1:p.Ile529Val
|
|