ENST00000402696.9:c.732G>T
MANE Select
|
ENSP00000385834.3:p.Leu244=
|
|
ENST00000402696.7:c.732G>T
|
ENSP00000385834.3:p.Leu244=
|
|
ENST00000482271.5:c.351G>T
|
ENSP00000419338.1:p.Leu117=
|
|
ENST00000485977.1:c.158-61G>T
|
ENSP00000418716.1:n.158-61G>T
|
|
NM_001063.3:c.732G>T
|
NP_001054.1:p.Leu244=
|
|
XM_011513100.1:c.732G>T
|
XP_011511402.1:p.Leu244=
|
|
NM_001354703.1:c.600G>T
|
NP_001341632.1:p.Leu200=
|
|
NM_001354704.1:c.351G>T
|
NP_001341633.1:p.Leu117=
|
|
NM_001063.4:c.732G>T
MANE Select
|
NP_001054.2:p.Leu244=
|
|
NM_001354703.2:c.600G>T
|
NP_001341632.2:p.Leu200=
|
|
NM_001354704.2:c.351G>T
|
NP_001341633.2:p.Leu117=
|
|