ENST00000303941.4:c.1267C>T
MANE Select
|
ENSP00000306678.3:p.Arg423Ter
|
|
ENST00000303941.3:c.1267C>T
|
ENSP00000306678.3:p.Arg423Ter
|
|
NM_178510.1:c.1267C>T
|
NP_848605.1:p.Arg423Ter
|
|
XM_011542736.1:c.1300C>T
|
XP_011541038.1:p.Arg434Ter
|
|
XM_011542737.1:c.1270C>T
|
XP_011541039.1:p.Arg424Ter
|
|
XM_011542738.1:c.1078C>T
|
XP_011541040.1:p.Arg360Ter
|
|
XM_011542736.2:c.1300C>T
|
XP_011541038.1:p.Arg434Ter
|
|
XM_011542737.2:c.1270C>T
|
XP_011541039.1:p.Arg424Ter
|
|
XM_011542738.2:c.1078C>T
|
XP_011541040.1:p.Arg360Ter
|
|
XM_017017475.1:c.1297C>T
|
XP_016872964.1:p.Arg433Ter
|
|
NM_178510.2:c.1267C>T
MANE Select
|
NP_848605.1:p.Arg423Ter
|
|