ENST00000326003.7:c.755G>T
MANE Select
|
ENSP00000314151.1:p.Trp252Leu
|
|
ENST00000326003.6:c.755G>T
|
ENSP00000314151.1:p.Trp252Leu
|
|
ENST00000360617.7:c.1197G>T
|
ENSP00000353829.2:n.1197G>T
|
|
ENST00000422986.6:c.*411G>T
|
ENSP00000393628.2:n.*411G>T
|
|
ENST00000595392.5:c.*256G>T
|
ENSP00000468912.1:n.*256G>T
|
|
ENST00000595952.5:c.626G>T
|
ENSP00000471155.1:p.Trp209Leu
|
|
ENST00000596333.1:n.933G>T
|
|
|
ENST00000598145.1:c.757G>T
|
|
|
ENST00000601349.5:n.2034G>T
|
|
|
ENST00000601812.1:n.1187G>T
|
|
|
ENST00000617027.4:c.632G>T
|
ENSP00000483513.1:p.Trp211Leu
|
|
NM_001030047.1:c.*480G>T
|
NP_001025218.1:n.*480G>T
|
|
NM_001030048.1:c.626G>T
|
NP_001025219.1:p.Trp209Leu
|
|
NM_001648.2:c.755G>T
MANE Select
|
NP_001639.1:p.Trp252Leu
|
|
XM_011526923.1:c.773G>T
|
XP_011525225.1:p.Trp258Leu
|
|
XR_935817.1:n.1324+842G>T
|
|
|