ENST00000342741.6:c.965G>C
MANE Select
|
ENSP00000339933.4:p.Arg322Thr
|
|
ENST00000342741.4:c.965G>C
|
ENSP00000339933.4:p.Arg322Thr
|
|
ENST00000392414.7:c.872G>C
|
ENSP00000376214.3:p.Arg291Thr
|
|
NM_000298.5:c.965G>C
|
NP_000289.1:p.Arg322Thr
|
|
NM_181871.3:c.872G>C
|
NP_870986.1:p.Arg291Thr
|
|
XM_005245266.3:c.1124G>C
|
XP_005245323.1:p.Arg375Thr
|
|
XM_006711386.2:c.773G>C
|
XP_006711449.1:p.Arg258Thr
|
|
XM_011509639.1:c.1124G>C
|
XP_011507941.1:p.Arg375Thr
|
|
XM_011509640.1:c.773G>C
|
XP_011507942.1:p.Arg258Thr
|
|
NM_000298.6:c.965G>C
MANE Select
|
NP_000289.1:p.Arg322Thr
|
|
XM_006711386.4:c.773G>C
|
XP_006711449.1:p.Arg258Thr
|
|
XM_011509640.3:c.773G>C
|
XP_011507942.1:p.Arg258Thr
|
|
XM_017001493.1:c.965G>C
|
XP_016856982.1:p.Arg322Thr
|
|
NM_181871.4:c.872G>C
|
NP_870986.1:p.Arg291Thr
|
|