ENST00000326003.7:c.782C>G
MANE Select
|
ENSP00000314151.1:p.Pro261Arg
|
|
ENST00000326003.6:c.782C>G
|
ENSP00000314151.1:p.Pro261Arg
|
|
ENST00000360617.7:c.1224C>G
|
ENSP00000353829.2:n.1224C>G
|
|
ENST00000422986.6:c.*438C>G
|
ENSP00000393628.2:n.*438C>G
|
|
ENST00000595392.5:c.*283C>G
|
ENSP00000468912.1:n.*283C>G
|
|
ENST00000595952.5:c.653C>G
|
ENSP00000471155.1:p.Pro218Arg
|
|
ENST00000596333.1:n.960C>G
|
|
|
ENST00000598145.1:c.784C>G
|
|
|
ENST00000601349.5:n.2061C>G
|
|
|
ENST00000601812.1:n.1214C>G
|
|
|
ENST00000617027.4:c.659C>G
|
ENSP00000483513.1:p.Pro220Arg
|
|
NM_001030047.1:c.*507C>G
|
NP_001025218.1:n.*507C>G
|
|
NM_001030048.1:c.653C>G
|
NP_001025219.1:p.Pro218Arg
|
|
NM_001648.2:c.782C>G
MANE Select
|
NP_001639.1:p.Pro261Arg
|
|
XM_011526923.1:c.800C>G
|
XP_011525225.1:p.Pro267Arg
|
|
XR_935817.1:n.1324+869C>G
|
|
|