ENST00000248633.9:c.2739A>G
MANE Select
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ENSP00000248633.4:p.Lys913=
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ENST00000248633.8:c.2739A>G
|
ENSP00000248633.4:p.Lys913=
|
|
ENST00000428214.5:c.2568A>G
|
ENSP00000394413.1:p.Lys856=
|
|
ENST00000438045.5:c.1773A>G
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ENSP00000410438.1:p.Lys591=
|
|
ENST00000484913.5:n.2778A>G
|
|
|
ENST00000496420.5:n.2631A>G
|
|
|
NM_000466.2:c.2739A>G
|
NP_000457.1:p.Lys913=
|
|
NM_001282677.1:c.2568A>G
|
NP_001269606.1:p.Lys856=
|
|
NM_001282678.1:c.2115A>G
|
NP_001269607.1:p.Lys705=
|
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XM_005250433.3:c.990A>G
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XP_005250490.1:p.Lys330=
|
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XR_242246.3:n.2835A>G
|
|
|
XM_017012319.2:c.990A>G
|
XP_016867808.1:p.Lys330=
|
|
XR_001744808.2:n.1766A>G
|
|
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XR_242246.5:n.2786A>G
|
|
|
NM_000466.3:c.2739A>G
MANE Select
|
NP_000457.1:p.Lys913=
|
|
NM_001282677.2:c.2568A>G
|
NP_001269606.1:p.Lys856=
|
|
NM_001282678.2:c.2115A>G
|
NP_001269607.1:p.Lys705=
|
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