ENST00000367698.4:c.1313G>C
MANE Select
|
ENSP00000356671.3:p.Arg438Thr
|
|
ENST00000367698.3:c.1313G>C
|
ENSP00000356671.3:p.Arg438Thr
|
|
ENST00000617423.4:c.698G>C
|
ENSP00000478688.1:p.Arg233Thr
|
|
NM_000488.3:c.1313G>C , LRG_577t1:c.1313G>C
|
NP_000479.1:p.Arg438Thr
|
|
XM_005245198.2:c.1169G>C
|
XP_005245255.1:p.Arg390Thr
|
|
NM_001365052.1:c.1169G>C
|
NP_001351981.1:p.Arg390Thr
|
|
NM_000488.4:c.1313G>C
MANE Select
|
NP_000479.1:p.Arg438Thr
|
|
NM_001365052.2:c.1169G>C
|
NP_001351981.1:p.Arg390Thr
|
|
NM_001386302.1:c.1436G>C
|
NP_001373231.1:p.Arg479Thr
|
|
NM_001386303.1:c.1394G>C
|
NP_001373232.1:p.Arg465Thr
|
|
NM_001386304.1:c.1292G>C
|
NP_001373233.1:p.Arg431Thr
|
|
NM_001386305.1:c.1256G>C
|
NP_001373234.1:p.Arg419Thr
|
|
NM_001386306.1:c.1097G>C
|
NP_001373235.1:p.Arg366Thr
|
|