ENST00000303941.4:c.1190C>G
MANE Select
|
ENSP00000306678.3:p.Thr397Arg
|
|
ENST00000303941.3:c.1190C>G
|
ENSP00000306678.3:p.Thr397Arg
|
|
NM_178510.1:c.1190C>G
|
NP_848605.1:p.Thr397Arg
|
|
XM_011542736.1:c.1223C>G
|
XP_011541038.1:p.Thr408Arg
|
|
XM_011542737.1:c.1193C>G
|
XP_011541039.1:p.Thr398Arg
|
|
XM_011542738.1:c.1001C>G
|
XP_011541040.1:p.Thr334Arg
|
|
XM_011542736.2:c.1223C>G
|
XP_011541038.1:p.Thr408Arg
|
|
XM_011542737.2:c.1193C>G
|
XP_011541039.1:p.Thr398Arg
|
|
XM_011542738.2:c.1001C>G
|
XP_011541040.1:p.Thr334Arg
|
|
XM_017017475.1:c.1220C>G
|
XP_016872964.1:p.Thr407Arg
|
|
NM_178510.2:c.1190C>G
MANE Select
|
NP_848605.1:p.Thr397Arg
|
|