ENST00000330062.8:c.449A=
MANE Select
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ENSP00000331897.4:p.Glu150=
|
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ENST00000330062.7:c.449A=
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ENSP00000331897.3:p.Glu150=
|
|
ENST00000540499.2:c.293A=
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ENSP00000446147.2:p.Glu98=
|
|
ENST00000559482.5:c.208-170A=
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ENSP00000453016.1:n.208-170A=
|
|
ENST00000560061.1:c.*74A=
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ENSP00000453254.1:n.*74A=
|
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NM_001289910.1:c.293A= , LRG_611t1:c.293A=
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NP_001276839.1:p.Glu98=
|
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NM_001290114.1:c.59A=
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NP_001277043.1:p.Glu20=
|
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NM_002168.3:c.449A= , LRG_611t2:c.449A=
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NP_002159.2:p.Glu150=
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NM_001290114.2:c.59A=
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NP_001277043.1:p.Glu20=
|
|
NM_002168.4:c.449A=
MANE Select
|
NP_002159.2:p.Glu150=
|
|