ENST00000258781.11:c.585G>C
MANE Select
|
ENSP00000258781.7:p.Leu195=
|
|
ENST00000648329.1:c.585G>C
|
ENSP00000496916.1:p.Leu195=
|
|
ENST00000258781.10:c.585G>C
|
ENSP00000258781.6:p.Leu195=
|
|
ENST00000381112.7:c.648G>C
|
ENSP00000370503.3:p.Leu216=
|
|
ENST00000461377.5:n.938G>C
|
|
|
ENST00000472223.5:n.652G>C
|
|
|
ENST00000474617.1:c.454+3909G>C
|
ENSP00000419474.1:n.454+3909G>C
|
|
ENST00000475551.5:c.567G>C
|
ENSP00000417180.1:p.Leu189=
|
|
ENST00000477605.1:n.920G>C
|
|
|
ENST00000478582.5:n.684-1271G>C
|
|
|
ENST00000480382.1:c.62G>C
|
|
|
ENST00000480658.5:n.413G>C
|
|
|
ENST00000481194.1:n.45-1271G>C
|
|
|
ENST00000482714.5:n.507G>C
|
|
|
ENST00000488727.5:c.585G>C
|
ENSP00000417251.1:p.Leu195=
|
|
ENST00000492883.5:n.485-1271G>C
|
|
|
ENST00000541586.5:c.411G>C
|
ENSP00000444725.1:p.Leu137=
|
|
ENST00000544363.5:c.472+3909G>C
|
ENSP00000438035.1:n.472+3909G>C
|
|
NM_001029835.2:c.648G>C , LRG_664t1:c.648G>C
|
NP_001025006.1:p.Leu216=
|
|
NM_001167934.1:c.411G>C
|
NP_001161406.1:p.Leu137=
|
|
NM_001167935.1:c.472+3909G>C
|
NP_001161407.1:n.472+3909G>C
|
|
NM_031443.3:c.585G>C , LRG_664t2:c.585G>C
|
NP_113631.1:p.Leu195=
|
|
NR_030770.1:n.667G>C
|
|
|
XM_006715785.2:c.474G>C
|
XP_006715848.1:p.Leu158=
|
|
XM_006715786.2:c.535+3909G>C
|
XP_006715849.1:n.535+3909G>C
|
|
XM_011515561.1:c.648G>C
|
XP_011513863.1:p.Leu216=
|
|
XM_011515562.1:c.585G>C
|
XP_011513864.1:p.Leu195=
|
|
XM_011515563.1:c.474G>C
|
XP_011513865.1:p.Leu158=
|
|
XM_011515564.1:c.411G>C
|
XP_011513866.1:p.Leu137=
|
|
XR_428088.2:n.661G>C
|
|
|
NM_001363458.1:c.585G>C
|
NP_001350387.1:p.Leu195=
|
|
NM_001363459.1:c.411G>C
|
NP_001350388.1:p.Leu137=
|
|
XM_006715785.4:c.474G>C
|
XP_006715848.1:p.Leu158=
|
|
XM_006715786.3:c.535+3909G>C
|
XP_006715849.1:n.535+3909G>C
|
|
XM_011515561.2:c.648G>C
|
XP_011513863.1:p.Leu216=
|
|
XM_011515563.3:c.474G>C
|
XP_011513865.1:p.Leu158=
|
|
XM_017012671.1:c.648G>C
|
XP_016868160.1:p.Leu216=
|
|
XM_017012672.2:c.474G>C
|
XP_016868161.1:p.Leu158=
|
|
XM_017012673.1:c.411G>C
|
XP_016868162.1:p.Leu137=
|
|
XR_428088.3:n.681G>C
|
|
|
NM_001363458.2:c.585G>C
|
NP_001350387.1:p.Leu195=
|
|
NM_001363459.2:c.411G>C
|
NP_001350388.1:p.Leu137=
|
|
NM_031443.4:c.585G>C
MANE Select
|
NP_113631.1:p.Leu195=
|
|
NR_030770.2:n.667G>C
|
|
|
NM_001167934.2:c.411G>C
|
NP_001161406.1:p.Leu137=
|
|
NM_001167935.2:c.472+3909G>C
|
NP_001161407.1:n.472+3909G>C
|
|