ENST00000326003.7:c.*30A>G
MANE Select
|
ENSP00000314151.1:n.*30A>G
|
|
ENST00000326003.6:c.*30A>G
|
ENSP00000314151.1:n.*30A>G
|
|
ENST00000360617.7:c.1258A>G
|
ENSP00000353829.2:n.1258A>G
|
|
ENST00000422986.6:c.*472A>G
|
ENSP00000393628.2:n.*472A>G
|
|
ENST00000595392.5:c.*317A>G
|
ENSP00000468912.1:n.*317A>G
|
|
ENST00000595952.5:c.*30A>G
|
ENSP00000471155.1:n.*30A>G
|
|
ENST00000596333.1:n.994A>G
|
|
|
ENST00000598145.1:c.818A>G
|
|
|
ENST00000601349.5:n.2095A>G
|
|
|
ENST00000617027.4:c.*30A>G
|
ENSP00000483513.1:n.*30A>G
|
|
NM_001030047.1:c.*541A>G
|
NP_001025218.1:n.*541A>G
|
|
NM_001030048.1:c.*30A>G
|
NP_001025219.1:n.*30A>G
|
|
NM_001648.2:c.*30A>G
MANE Select
|
NP_001639.1:n.*30A>G
|
|
XM_011526923.1:c.*30A>G
|
XP_011525225.1:n.*30A>G
|
|
XR_935817.1:n.1324+903A>G
|
|
|