ENST00000326003.7:c.738G>T
MANE Select
|
ENSP00000314151.1:p.Val246=
|
|
ENST00000326003.6:c.738G>T
|
ENSP00000314151.1:p.Val246=
|
|
ENST00000360617.7:c.1180G>T
|
ENSP00000353829.2:n.1180G>T
|
|
ENST00000422986.6:c.*394G>T
|
ENSP00000393628.2:n.*394G>T
|
|
ENST00000595392.5:c.*239G>T
|
ENSP00000468912.1:n.*239G>T
|
|
ENST00000595952.5:c.609G>T
|
ENSP00000471155.1:p.Val203=
|
|
ENST00000596333.1:n.916G>T
|
|
|
ENST00000598145.1:c.740G>T
|
|
|
ENST00000601349.5:n.2017G>T
|
|
|
ENST00000601812.1:n.1170G>T
|
|
|
ENST00000617027.4:c.615G>T
|
ENSP00000483513.1:p.Val205=
|
|
NM_001030047.1:c.*463G>T
|
NP_001025218.1:n.*463G>T
|
|
NM_001030048.1:c.609G>T
|
NP_001025219.1:p.Val203=
|
|
NM_001648.2:c.738G>T
MANE Select
|
NP_001639.1:p.Val246=
|
|
XM_011526923.1:c.756G>T
|
XP_011525225.1:p.Val252=
|
|
XR_935817.1:n.1324+825G>T
|
|
|