ENST00000367698.4:c.1292G>C
MANE Select
|
ENSP00000356671.3:p.Arg431Thr
|
|
ENST00000367698.3:c.1292G>C
|
ENSP00000356671.3:p.Arg431Thr
|
|
ENST00000617423.4:c.677G>C
|
ENSP00000478688.1:p.Arg226Thr
|
|
NM_000488.3:c.1292G>C , LRG_577t1:c.1292G>C
|
NP_000479.1:p.Arg431Thr
|
|
XM_005245198.2:c.1148G>C
|
XP_005245255.1:p.Arg383Thr
|
|
NM_001365052.1:c.1148G>C
|
NP_001351981.1:p.Arg383Thr
|
|
NM_000488.4:c.1292G>C
MANE Select
|
NP_000479.1:p.Arg431Thr
|
|
NM_001365052.2:c.1148G>C
|
NP_001351981.1:p.Arg383Thr
|
|
NM_001386302.1:c.1415G>C
|
NP_001373231.1:p.Arg472Thr
|
|
NM_001386303.1:c.1373G>C
|
NP_001373232.1:p.Arg458Thr
|
|
NM_001386304.1:c.1271G>C
|
NP_001373233.1:p.Arg424Thr
|
|
NM_001386305.1:c.1235G>C
|
NP_001373234.1:p.Arg412Thr
|
|
NM_001386306.1:c.1076G>C
|
NP_001373235.1:p.Arg359Thr
|
|