ENST00000248633.9:c.2072C>G
MANE Select
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ENSP00000248633.4:p.Ala691Gly
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ENST00000248633.8:c.2072C>G
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ENSP00000248633.4:p.Ala691Gly
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|
ENST00000428214.5:c.1901C>G
|
ENSP00000394413.1:p.Ala634Gly
|
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ENST00000438045.5:c.1106C>G
|
ENSP00000410438.1:p.Ala369Gly
|
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ENST00000484913.5:n.2111C>G
|
|
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ENST00000496420.5:n.1748C>G
|
|
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NM_000466.2:c.2072C>G
|
NP_000457.1:p.Ala691Gly
|
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NM_001282677.1:c.1901C>G
|
NP_001269606.1:p.Ala634Gly
|
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NM_001282678.1:c.1448C>G
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NP_001269607.1:p.Ala483Gly
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XM_005250433.3:c.323C>G
|
XP_005250490.1:p.Ala108Gly
|
|
XR_242246.3:n.2168C>G
|
|
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XM_017012319.2:c.323C>G
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XP_016867808.1:p.Ala108Gly
|
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XR_001744808.2:n.1099C>G
|
|
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XR_242246.5:n.2119C>G
|
|
|
NM_000466.3:c.2072C>G
MANE Select
|
NP_000457.1:p.Ala691Gly
|
|
NM_001282677.2:c.1901C>G
|
NP_001269606.1:p.Ala634Gly
|
|
NM_001282678.2:c.1448C>G
|
NP_001269607.1:p.Ala483Gly
|
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