ENST00000367698.4:c.1314G>C
MANE Select
|
ENSP00000356671.3:p.Arg438Ser
|
|
ENST00000367698.3:c.1314G>C
|
ENSP00000356671.3:p.Arg438Ser
|
|
ENST00000617423.4:c.699G>C
|
ENSP00000478688.1:p.Arg233Ser
|
|
NM_000488.3:c.1314G>C , LRG_577t1:c.1314G>C
|
NP_000479.1:p.Arg438Ser
|
|
XM_005245198.2:c.1170G>C
|
XP_005245255.1:p.Arg390Ser
|
|
NM_001365052.1:c.1170G>C
|
NP_001351981.1:p.Arg390Ser
|
|
NM_000488.4:c.1314G>C
MANE Select
|
NP_000479.1:p.Arg438Ser
|
|
NM_001365052.2:c.1170G>C
|
NP_001351981.1:p.Arg390Ser
|
|
NM_001386302.1:c.1437G>C
|
NP_001373231.1:p.Arg479Ser
|
|
NM_001386303.1:c.1395G>C
|
NP_001373232.1:p.Arg465Ser
|
|
NM_001386304.1:c.1293G>C
|
NP_001373233.1:p.Arg431Ser
|
|
NM_001386305.1:c.1257G>C
|
NP_001373234.1:p.Arg419Ser
|
|
NM_001386306.1:c.1098G>C
|
NP_001373235.1:p.Arg366Ser
|
|