ENST00000326003.7:c.*99T>C
MANE Select
|
ENSP00000314151.1:n.*99T>C
|
|
ENST00000326003.6:c.*99T>C
|
ENSP00000314151.1:n.*99T>C
|
|
ENST00000360617.7:c.1327T>C
|
ENSP00000353829.2:n.1327T>C
|
|
ENST00000422986.6:c.*541T>C
|
ENSP00000393628.2:n.*541T>C
|
|
ENST00000595392.5:c.*386T>C
|
ENSP00000468912.1:n.*386T>C
|
|
ENST00000595952.5:c.*99T>C
|
ENSP00000471155.1:n.*99T>C
|
|
ENST00000596333.1:n.1063T>C
|
|
|
ENST00000601349.5:n.2164T>C
|
|
|
ENST00000617027.4:c.*99T>C
|
ENSP00000483513.1:n.*99T>C
|
|
NM_001030047.1:c.*610T>C
|
NP_001025218.1:n.*610T>C
|
|
NM_001030048.1:c.*99T>C
|
NP_001025219.1:n.*99T>C
|
|
NM_001648.2:c.*99T>C
MANE Select
|
NP_001639.1:n.*99T>C
|
|
XM_011526923.1:c.*99T>C
|
XP_011525225.1:n.*99T>C
|
|
XR_935817.1:n.1324+972T>C
|
|
|