ENST00000248633.9:c.2756A>T
MANE Select
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ENSP00000248633.4:p.Glu919Val
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ENST00000248633.8:c.2756A>T
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ENSP00000248633.4:p.Glu919Val
|
|
ENST00000428214.5:c.2585A>T
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ENSP00000394413.1:p.Glu862Val
|
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ENST00000438045.5:c.1790A>T
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ENSP00000410438.1:p.Glu597Val
|
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ENST00000484913.5:n.2795A>T
|
|
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ENST00000496420.5:n.2648A>T
|
|
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NM_000466.2:c.2756A>T
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NP_000457.1:p.Glu919Val
|
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NM_001282677.1:c.2585A>T
|
NP_001269606.1:p.Glu862Val
|
|
NM_001282678.1:c.2132A>T
|
NP_001269607.1:p.Glu711Val
|
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XM_005250433.3:c.1007A>T
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XP_005250490.1:p.Glu336Val
|
|
XR_242246.3:n.2852A>T
|
|
|
XM_017012319.2:c.1007A>T
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XP_016867808.1:p.Glu336Val
|
|
XR_001744808.2:n.1783A>T
|
|
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XR_242246.5:n.2803A>T
|
|
|
NM_000466.3:c.2756A>T
MANE Select
|
NP_000457.1:p.Glu919Val
|
|
NM_001282677.2:c.2585A>T
|
NP_001269606.1:p.Glu862Val
|
|
NM_001282678.2:c.2132A>T
|
NP_001269607.1:p.Glu711Val
|
|