ENST00000248633.9:c.2389T=
MANE Select
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ENSP00000248633.4:p.Ser797=
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|
ENST00000248633.8:c.2389T=
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ENSP00000248633.4:p.Ser797=
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|
ENST00000428214.5:c.2218T=
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ENSP00000394413.1:p.Ser740=
|
|
ENST00000438045.5:c.1423T=
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ENSP00000410438.1:p.Ser475=
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ENST00000484913.5:n.2428T=
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|
|
ENST00000496092.1:n.187T=
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|
|
ENST00000496420.5:n.2065T=
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|
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NM_000466.2:c.2389T=
|
NP_000457.1:p.Ser797=
|
|
NM_001282677.1:c.2218T=
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NP_001269606.1:p.Ser740=
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|
NM_001282678.1:c.1765T=
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NP_001269607.1:p.Ser589=
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XM_005250433.3:c.640T=
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XP_005250490.1:p.Ser214=
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|
XR_242246.3:n.2485T=
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|
|
XM_017012319.2:c.640T=
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XP_016867808.1:p.Ser214=
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|
XR_001744808.2:n.1416T=
|
|
|
XR_242246.5:n.2436T=
|
|
|
NM_000466.3:c.2389T=
MANE Select
|
NP_000457.1:p.Ser797=
|
|
NM_001282677.2:c.2218T=
|
NP_001269606.1:p.Ser740=
|
|
NM_001282678.2:c.1765T=
|
NP_001269607.1:p.Ser589=
|
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