ENST00000315491.12:c.1083C>T
MANE Select
|
ENSP00000320295.7:p.Leu361=
|
|
ENST00000680788.1:n.4504C>T
|
|
|
ENST00000315491.11:c.1083C>T
|
ENSP00000320295.7:p.Leu361=
|
|
ENST00000554444.5:c.867C>T
|
ENSP00000451617.1:p.Leu289=
|
|
ENST00000555576.5:c.277+1956C>T
|
ENSP00000452554.1:n.277+1956C>T
|
|
ENST00000555609.5:c.*1168C>T
|
ENSP00000451276.1:n.*1168C>T
|
|
ENST00000556922.1:c.2124C>T
|
ENSP00000451560.1:p.Leu708=
|
|
NM_001197181.1:c.867C>T
|
NP_001184110.1:p.Leu289=
|
|
NM_006086.3:c.1083C>T
|
NP_006077.2:p.Leu361=
|
|
NM_006086.4:c.1083C>T
MANE Select
|
NP_006077.2:p.Leu361=
|
|
NM_001197181.2:c.867C>T
|
NP_001184110.1:p.Leu289=
|
|