ENST00000315491.12:c.684G>T
MANE Select
|
ENSP00000320295.7:p.Leu228=
|
|
ENST00000680788.1:n.4105G>T
|
|
|
ENST00000315491.11:c.684G>T
|
ENSP00000320295.7:p.Leu228=
|
|
ENST00000554444.5:c.468G>T
|
ENSP00000451617.1:p.Leu156=
|
|
ENST00000555576.5:c.277+1557G>T
|
ENSP00000452554.1:n.277+1557G>T
|
|
ENST00000555609.5:c.*769G>T
|
ENSP00000451276.1:n.*769G>T
|
|
ENST00000555810.5:c.468G>T
|
ENSP00000450538.1:p.Leu156=
|
|
ENST00000556922.1:c.1725G>T
|
ENSP00000451560.1:p.Leu575=
|
|
NM_001197181.1:c.468G>T
|
NP_001184110.1:p.Leu156=
|
|
NM_006086.3:c.684G>T
|
NP_006077.2:p.Leu228=
|
|
NM_006086.4:c.684G>T
MANE Select
|
NP_006077.2:p.Leu228=
|
|
NM_001197181.2:c.468G>T
|
NP_001184110.1:p.Leu156=
|
|