ENST00000625662.3:c.2141A=
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|
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ENST00000628118.2:c.1668A=
|
|
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ENST00000700551.1:c.*1465A=
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ENSP00000515057.1:n.*1465A=
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|
ENST00000394196.9:c.2634A=
MANE Select
|
ENSP00000377747.4:p.Ser878=
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|
ENST00000635856.1:n.3206A=
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|
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ENST00000636306.1:n.194A=
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|
|
ENST00000636881.1:c.2005A=
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|
|
ENST00000637572.1:n.3378A=
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|
|
ENST00000394196.8:c.2634A=
|
ENSP00000377747.4:p.Ser878=
|
|
ENST00000625463.1:c.174A=
|
ENSP00000486391.1:p.Ser58=
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|
ENST00000626874.2:c.2634A=
|
ENSP00000486629.1:p.Ser878=
|
|
ENST00000628118.1:n.413A=
|
|
|
NM_001271.3:c.2634A=
|
NP_001262.3:p.Ser878=
|
|
NM_001271.4:c.2634A=
MANE Select
|
NP_001262.3:p.Ser878=
|
|