ENST00000303941.4:c.1136G>C
MANE Select
|
ENSP00000306678.3:p.Arg379Thr
|
|
ENST00000303941.3:c.1136G>C
|
ENSP00000306678.3:p.Arg379Thr
|
|
NM_178510.1:c.1136G>C
|
NP_848605.1:p.Arg379Thr
|
|
XM_011542736.1:c.1169G>C
|
XP_011541038.1:p.Arg390Thr
|
|
XM_011542737.1:c.1139G>C
|
XP_011541039.1:p.Arg380Thr
|
|
XM_011542738.1:c.947G>C
|
XP_011541040.1:p.Arg316Thr
|
|
XM_011542736.2:c.1169G>C
|
XP_011541038.1:p.Arg390Thr
|
|
XM_011542737.2:c.1139G>C
|
XP_011541039.1:p.Arg380Thr
|
|
XM_011542738.2:c.947G>C
|
XP_011541040.1:p.Arg316Thr
|
|
XM_017017475.1:c.1166G>C
|
XP_016872964.1:p.Arg389Thr
|
|
NM_178510.2:c.1136G>C
MANE Select
|
NP_848605.1:p.Arg379Thr
|
|