ENST00000393609.8:c.798G>C
MANE Select
|
ENSP00000377233.3:p.Leu266=
|
|
ENST00000334211.12:c.63G>C
|
ENSP00000335506.8:p.Leu21=
|
|
ENST00000359373.9:c.798G>C
|
ENSP00000352332.5:p.Leu266=
|
|
ENST00000393605.7:c.78G>C
|
ENSP00000377230.3:p.Leu26=
|
|
ENST00000393609.7:c.798G>C
|
ENSP00000377233.3:p.Leu266=
|
|
ENST00000426523.5:c.63G>C
|
ENSP00000392264.1:p.Leu21=
|
|
ENST00000429686.5:c.63G>C
|
ENSP00000403127.1:p.Leu21=
|
|
ENST00000465814.5:n.1135G>C
|
|
|
NM_001040118.2:c.798G>C
|
NP_001035207.1:p.Leu266=
|
|
NM_001135190.1:c.63G>C
|
NP_001128662.1:p.Leu21=
|
|
NM_015242.4:c.63G>C
|
NP_056057.2:p.Leu21=
|
|
NM_001369489.1:c.63G>C
|
NP_001356418.1:p.Leu21=
|
|
NR_161388.1:n.780G>C
|
|
|
NM_001040118.3:c.798G>C
MANE Select
|
NP_001035207.1:p.Leu266=
|
|
NM_001135190.2:c.63G>C
|
NP_001128662.1:p.Leu21=
|
|
NM_015242.5:c.63G>C
|
NP_056057.2:p.Leu21=
|
|