ENST00000248633.9:c.2632C>A
MANE Select
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ENSP00000248633.4:p.Leu878Met
|
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ENST00000248633.8:c.2632C>A
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ENSP00000248633.4:p.Leu878Met
|
|
ENST00000428214.5:c.2461C>A
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ENSP00000394413.1:p.Leu821Met
|
|
ENST00000438045.5:c.1666C>A
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ENSP00000410438.1:p.Leu556Met
|
|
ENST00000484913.5:n.2671C>A
|
|
|
ENST00000496420.5:n.2524C>A
|
|
|
NM_000466.2:c.2632C>A
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NP_000457.1:p.Leu878Met
|
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NM_001282677.1:c.2461C>A
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NP_001269606.1:p.Leu821Met
|
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NM_001282678.1:c.2008C>A
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NP_001269607.1:p.Leu670Met
|
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XM_005250433.3:c.883C>A
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XP_005250490.1:p.Leu295Met
|
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XR_242246.3:n.2728C>A
|
|
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XM_017012319.2:c.883C>A
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XP_016867808.1:p.Leu295Met
|
|
XR_001744808.2:n.1659C>A
|
|
|
XR_242246.5:n.2679C>A
|
|
|
NM_000466.3:c.2632C>A
MANE Select
|
NP_000457.1:p.Leu878Met
|
|
NM_001282677.2:c.2461C>A
|
NP_001269606.1:p.Leu821Met
|
|
NM_001282678.2:c.2008C>A
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NP_001269607.1:p.Leu670Met
|
|