ENST00000326003.7:c.*238G>T
MANE Select
|
ENSP00000314151.1:n.*238G>T
|
|
ENST00000326003.6:c.*238G>T
|
ENSP00000314151.1:n.*238G>T
|
|
ENST00000360617.7:c.1466G>T
|
ENSP00000353829.2:n.1466G>T
|
|
ENST00000422986.6:c.*680G>T
|
ENSP00000393628.2:n.*680G>T
|
|
ENST00000595952.5:c.*238G>T
|
ENSP00000471155.1:n.*238G>T
|
|
ENST00000596333.1:n.1202G>T
|
|
|
ENST00000601349.5:n.2303G>T
|
|
|
ENST00000617027.4:c.*238G>T
|
ENSP00000483513.1:n.*238G>T
|
|
NM_001030047.1:c.*749G>T
|
NP_001025218.1:n.*749G>T
|
|
NM_001030048.1:c.*238G>T
|
NP_001025219.1:n.*238G>T
|
|
NM_001648.2:c.*238G>T
MANE Select
|
NP_001639.1:n.*238G>T
|
|
XM_011526923.1:c.*238G>T
|
XP_011525225.1:n.*238G>T
|
|
XR_935817.1:n.1324+1111G>T
|
|
|