ENST00000326003.7:c.*295G>T
MANE Select
|
ENSP00000314151.1:n.*295G>T
|
|
ENST00000326003.6:c.*295G>T
|
ENSP00000314151.1:n.*295G>T
|
|
ENST00000360617.7:c.1523G>T
|
ENSP00000353829.2:n.1523G>T
|
|
ENST00000422986.6:c.*737G>T
|
ENSP00000393628.2:n.*737G>T
|
|
ENST00000595952.5:c.*295G>T
|
ENSP00000471155.1:n.*295G>T
|
|
ENST00000596333.1:n.1259G>T
|
|
|
ENST00000601349.5:n.2360G>T
|
|
|
ENST00000617027.4:c.*295G>T
|
ENSP00000483513.1:n.*295G>T
|
|
NM_001030047.1:c.*806G>T
|
NP_001025218.1:n.*806G>T
|
|
NM_001030048.1:c.*295G>T
|
NP_001025219.1:n.*295G>T
|
|
NM_001648.2:c.*295G>T
MANE Select
|
NP_001639.1:n.*295G>T
|
|
XM_011526923.1:c.*295G>T
|
XP_011525225.1:n.*295G>T
|
|
XR_935817.1:n.1324+1168G>T
|
|
|