ENST00000315491.12:c.1352G=
MANE Select
|
ENSP00000320295.7:p.Ter451=
|
|
ENST00000680788.1:n.4773G=
|
|
|
ENST00000315491.11:c.1352G=
|
ENSP00000320295.7:p.Ter451=
|
|
ENST00000554444.5:c.1136G=
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ENSP00000451617.1:p.Ter379=
|
|
ENST00000555576.5:c.277+2225G=
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ENSP00000452554.1:n.277+2225G=
|
|
ENST00000555609.5:c.*1437G=
|
ENSP00000451276.1:n.*1437G=
|
|
ENST00000556922.1:c.2393G=
|
ENSP00000451560.1:p.Ter798=
|
|
NM_001197181.1:c.1136G=
|
NP_001184110.1:p.Ter379=
|
|
NM_006086.3:c.1352G=
|
NP_006077.2:p.Ter451=
|
|
NM_006086.4:c.1352G=
MANE Select
|
NP_006077.2:p.Ter451=
|
|
NM_001197181.2:c.1136G=
|
NP_001184110.1:p.Ter379=
|
|