ENST00000367698.4:c.1130G>C
MANE Select
|
ENSP00000356671.3:p.Ser377Thr
|
|
ENST00000367698.3:c.1130G>C
|
ENSP00000356671.3:p.Ser377Thr
|
|
ENST00000617423.4:c.560-2082G>C
|
ENSP00000478688.1:n.560-2082G>C
|
|
NM_000488.3:c.1130G>C , LRG_577t1:c.1130G>C
|
NP_000479.1:p.Ser377Thr
|
|
XM_005245198.2:c.986G>C
|
XP_005245255.1:p.Ser329Thr
|
|
NM_001365052.1:c.986G>C
|
NP_001351981.1:p.Ser329Thr
|
|
NM_000488.4:c.1130G>C
MANE Select
|
NP_000479.1:p.Ser377Thr
|
|
NM_001365052.2:c.986G>C
|
NP_001351981.1:p.Ser329Thr
|
|
NM_001386302.1:c.1253G>C
|
NP_001373231.1:p.Ser418Thr
|
|
NM_001386303.1:c.1211G>C
|
NP_001373232.1:p.Ser404Thr
|
|
NM_001386304.1:c.1109G>C
|
NP_001373233.1:p.Ser370Thr
|
|
NM_001386305.1:c.1073G>C
|
NP_001373234.1:p.Ser358Thr
|
|
NM_001386306.1:c.914G>C
|
NP_001373235.1:p.Ser305Thr
|
|