ENST00000304874.14:c.655G>T
MANE Select
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ENSP00000307188.9:p.Glu219Ter
|
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ENST00000362000.10:c.460G>T
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ENSP00000354710.6:p.Glu154Ter
|
|
ENST00000380839.9:c.577G>T
|
ENSP00000370219.4:p.Glu193Ter
|
|
ENST00000395331.4:c.655G>T
|
ENSP00000378740.3:p.Glu219Ter
|
|
ENST00000395332.8:c.655G>T
|
ENSP00000378741.3:p.Glu219Ter
|
|
ENST00000671817.1:c.577G>T
|
ENSP00000500462.1:p.Glu193Ter
|
|
ENST00000672498.1:c.447-343G>T
|
ENSP00000500227.1:n.447-343G>T
|
|
ENST00000672586.1:n.1072G>T
|
|
|
ENST00000672676.1:n.1337G>T
|
|
|
ENST00000673149.1:n.467G>T
|
|
|
ENST00000673350.1:n.1415G>T
|
|
|
ENST00000673518.1:c.577G>T
|
ENSP00000499889.1:p.Glu193Ter
|
|
ENST00000673594.1:n.504G>T
|
|
|
ENST00000304874.13:c.655G>T
|
ENSP00000307188.9:p.Glu219Ter
|
|
ENST00000362000.9:c.460G>T
|
ENSP00000354710.5:p.Glu154Ter
|
|
ENST00000380839.8:c.577G>T
|
ENSP00000370219.4:p.Glu193Ter
|
|
ENST00000395331.3:c.655G>T
|
ENSP00000378740.3:p.Glu219Ter
|
|
ENST00000395332.7:c.655G>T
|
ENSP00000378741.3:p.Glu219Ter
|
|
NM_000048.3:c.655G>T
|
NP_000039.2:p.Glu219Ter
|
|
NM_001024943.1:c.655G>T
|
NP_001020114.1:p.Glu219Ter
|
|
NM_001024944.1:c.655G>T
|
NP_001020115.1:p.Glu219Ter
|
|
NM_001024946.1:c.577G>T
|
NP_001020117.1:p.Glu193Ter
|
|
NM_000048.4:c.655G>T
MANE Select
|
NP_000039.2:p.Glu219Ter
|
|
NM_001024943.2:c.655G>T
|
NP_001020114.1:p.Glu219Ter
|
|
NM_001024944.2:c.655G>T
|
NP_001020115.1:p.Glu219Ter
|
|
NM_001024946.2:c.577G>T
|
NP_001020117.1:p.Glu193Ter
|
|