ENST00000315491.12:c.696C>G
MANE Select
|
ENSP00000320295.7:p.Thr232=
|
|
ENST00000680788.1:n.4117C>G
|
|
|
ENST00000315491.11:c.696C>G
|
ENSP00000320295.7:p.Thr232=
|
|
ENST00000554444.5:c.480C>G
|
ENSP00000451617.1:p.Thr160=
|
|
ENST00000555576.5:c.277+1569C>G
|
ENSP00000452554.1:n.277+1569C>G
|
|
ENST00000555609.5:c.*781C>G
|
ENSP00000451276.1:n.*781C>G
|
|
ENST00000555810.5:c.480C>G
|
ENSP00000450538.1:p.Thr160=
|
|
ENST00000556922.1:c.1737C>G
|
ENSP00000451560.1:p.Thr579=
|
|
NM_001197181.1:c.480C>G
|
NP_001184110.1:p.Thr160=
|
|
NM_006086.3:c.696C>G
|
NP_006077.2:p.Thr232=
|
|
NM_006086.4:c.696C>G
MANE Select
|
NP_006077.2:p.Thr232=
|
|
NM_001197181.2:c.480C>G
|
NP_001184110.1:p.Thr160=
|
|