ENST00000562435.6:c.1532G>C
MANE Select
|
ENSP00000455169.1:p.Arg511Thr
|
|
ENST00000303155.9:c.1511G>C
|
ENSP00000306726.5:p.Arg504Thr
|
|
ENST00000562435.5:c.1532G>C
|
ENSP00000455169.1:p.Arg511Thr
|
|
ENST00000562559.5:c.1050G>C
|
|
|
ENST00000564667.1:c.639G>C
|
|
|
NM_001201477.1:c.1511G>C
|
NP_001188406.1:p.Arg504Thr
|
|
NM_018092.4:c.1532G>C
|
NP_060562.3:p.Arg511Thr
|
|
XM_006721289.1:c.1418G>C
|
XP_006721352.1:p.Arg473Thr
|
|
XM_006721291.1:c.1397G>C
|
XP_006721354.1:p.Arg466Thr
|
|
XM_017023740.1:c.1124G>C
|
XP_016879229.1:p.Arg375Thr
|
|
NM_001201477.2:c.1511G>C
|
NP_001188406.1:p.Arg504Thr
|
|
NM_018092.5:c.1532G>C
MANE Select
|
NP_060562.3:p.Arg511Thr
|
|