ENST00000326003.7:c.708G>T
MANE Select
|
ENSP00000314151.1:p.Leu236=
|
|
ENST00000326003.6:c.708G>T
|
ENSP00000314151.1:p.Leu236=
|
|
ENST00000360617.7:c.1150G>T
|
ENSP00000353829.2:n.1150G>T
|
|
ENST00000422986.6:c.*364G>T
|
ENSP00000393628.2:n.*364G>T
|
|
ENST00000595392.5:c.*209G>T
|
ENSP00000468912.1:n.*209G>T
|
|
ENST00000595952.5:c.579G>T
|
ENSP00000471155.1:p.Leu193=
|
|
ENST00000596333.1:n.886G>T
|
|
|
ENST00000598145.1:c.710G>T
|
|
|
ENST00000601349.5:n.1987G>T
|
|
|
ENST00000601812.1:n.1140G>T
|
|
|
ENST00000617027.4:c.585G>T
|
ENSP00000483513.1:p.Leu195=
|
|
NM_001030047.1:c.*433G>T
|
NP_001025218.1:n.*433G>T
|
|
NM_001030048.1:c.579G>T
|
NP_001025219.1:p.Leu193=
|
|
NM_001648.2:c.708G>T
MANE Select
|
NP_001639.1:p.Leu236=
|
|
XM_011526923.1:c.726G>T
|
XP_011525225.1:p.Leu242=
|
|
XR_935817.1:n.1324+795G>T
|
|
|