ENST00000326003.7:c.*48G>A
MANE Select
|
ENSP00000314151.1:n.*48G>A
|
|
ENST00000326003.6:c.*48G>A
|
ENSP00000314151.1:n.*48G>A
|
|
ENST00000360617.7:c.1276G>A
|
ENSP00000353829.2:n.1276G>A
|
|
ENST00000422986.6:c.*490G>A
|
ENSP00000393628.2:n.*490G>A
|
|
ENST00000595392.5:c.*335G>A
|
ENSP00000468912.1:n.*335G>A
|
|
ENST00000595952.5:c.*48G>A
|
ENSP00000471155.1:n.*48G>A
|
|
ENST00000596333.1:n.1012G>A
|
|
|
ENST00000598145.1:c.836G>A
|
|
|
ENST00000601349.5:n.2113G>A
|
|
|
ENST00000617027.4:c.*48G>A
|
ENSP00000483513.1:n.*48G>A
|
|
NM_001030047.1:c.*559G>A
|
NP_001025218.1:n.*559G>A
|
|
NM_001030048.1:c.*48G>A
|
NP_001025219.1:n.*48G>A
|
|
NM_001648.2:c.*48G>A
MANE Select
|
NP_001639.1:n.*48G>A
|
|
XM_011526923.1:c.*48G>A
|
XP_011525225.1:n.*48G>A
|
|
XR_935817.1:n.1324+921G>A
|
|
|