ENST00000326003.7:c.771C=
MANE Select
|
ENSP00000314151.1:p.Ile257=
|
|
ENST00000326003.6:c.771C=
|
ENSP00000314151.1:p.Ile257=
|
|
ENST00000360617.7:c.1213C=
|
ENSP00000353829.2:n.1213C=
|
|
ENST00000422986.6:c.*427C=
|
ENSP00000393628.2:n.*427C=
|
|
ENST00000595392.5:c.*272C=
|
ENSP00000468912.1:n.*272C=
|
|
ENST00000595952.5:c.642C=
|
ENSP00000471155.1:p.Ile214=
|
|
ENST00000596333.1:n.949C=
|
|
|
ENST00000598145.1:c.773C=
|
|
|
ENST00000601349.5:n.2050C=
|
|
|
ENST00000601812.1:n.1203C=
|
|
|
ENST00000617027.4:c.648C=
|
ENSP00000483513.1:p.Ile216=
|
|
NM_001030047.1:c.*496C=
|
NP_001025218.1:n.*496C=
|
|
NM_001030048.1:c.642C=
|
NP_001025219.1:p.Ile214=
|
|
NM_001648.2:c.771C=
MANE Select
|
NP_001639.1:p.Ile257=
|
|
XM_011526923.1:c.789C=
|
XP_011525225.1:p.Ile263=
|
|
XR_935817.1:n.1324+858C=
|
|
|