ENST00000340855.11:c.947G=
MANE Select
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ENSP00000339801.6:p.Ser316=
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|
ENST00000651111.1:c.314G=
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ENSP00000498395.1:p.Ser105=
|
|
ENST00000340855.10:c.947G=
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ENSP00000339801.6:p.Ser316=
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|
ENST00000370441.8:c.947G=
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ENSP00000359470.4:p.Ser316=
|
|
ENST00000422081.6:c.314G=
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ENSP00000477056.1:p.Ser105=
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|
ENST00000441880.1:n.114-3275G=
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|
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ENST00000464251.5:c.873G=
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ENSP00000428980.1:n.873G=
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|
ENST00000466323.5:c.*138G=
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ENSP00000418264.1:n.*138G=
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ENST00000490775.5:n.732G=
|
|
|
NM_000202.6:c.947G=
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NP_000193.1:p.Ser316=
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|
NM_001166550.2:c.677G=
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NP_001160022.1:p.Ser226=
|
|
NM_006123.4:c.947G=
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NP_006114.1:p.Ser316=
|
|
NR_104128.1:n.1294G=
|
|
|
NM_000202.7:c.947G=
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NP_000193.1:p.Ser316=
|
|
NM_001166550.3:c.677G=
|
NP_001160022.1:p.Ser226=
|
|
NM_000202.8:c.947G=
MANE Select
|
NP_000193.1:p.Ser316=
|
|
NM_001166550.4:c.677G=
|
NP_001160022.1:p.Ser226=
|
|
NM_006123.5:c.947G=
|
NP_006114.1:p.Ser316=
|
|
NR_104128.2:n.1246G=
|
|
|