ENST00000326003.7:c.*66G>A
MANE Select
|
ENSP00000314151.1:n.*66G>A
|
|
ENST00000326003.6:c.*66G>A
|
ENSP00000314151.1:n.*66G>A
|
|
ENST00000360617.7:c.1294G>A
|
ENSP00000353829.2:n.1294G>A
|
|
ENST00000422986.6:c.*508G>A
|
ENSP00000393628.2:n.*508G>A
|
|
ENST00000595392.5:c.*353G>A
|
ENSP00000468912.1:n.*353G>A
|
|
ENST00000595952.5:c.*66G>A
|
ENSP00000471155.1:n.*66G>A
|
|
ENST00000596333.1:n.1030G>A
|
|
|
ENST00000598145.1:c.854G>A
|
|
|
ENST00000601349.5:n.2131G>A
|
|
|
ENST00000617027.4:c.*66G>A
|
ENSP00000483513.1:n.*66G>A
|
|
NM_001030047.1:c.*577G>A
|
NP_001025218.1:n.*577G>A
|
|
NM_001030048.1:c.*66G>A
|
NP_001025219.1:n.*66G>A
|
|
NM_001648.2:c.*66G>A
MANE Select
|
NP_001639.1:n.*66G>A
|
|
XM_011526923.1:c.*66G>A
|
XP_011525225.1:n.*66G>A
|
|
XR_935817.1:n.1324+939G>A
|
|
|