ENST00000367698.4:c.1276T>A
MANE Select
|
ENSP00000356671.3:p.Ser426Thr
|
|
ENST00000367698.3:c.1276T>A
|
ENSP00000356671.3:p.Ser426Thr
|
|
ENST00000617423.4:c.661T>A
|
ENSP00000478688.1:p.Ser221Thr
|
|
NM_000488.3:c.1276T>A , LRG_577t1:c.1276T>A
|
NP_000479.1:p.Ser426Thr
|
|
XM_005245198.2:c.1132T>A
|
XP_005245255.1:p.Ser378Thr
|
|
NM_001365052.1:c.1132T>A
|
NP_001351981.1:p.Ser378Thr
|
|
NM_000488.4:c.1276T>A
MANE Select
|
NP_000479.1:p.Ser426Thr
|
|
NM_001365052.2:c.1132T>A
|
NP_001351981.1:p.Ser378Thr
|
|
NM_001386302.1:c.1399T>A
|
NP_001373231.1:p.Ser467Thr
|
|
NM_001386303.1:c.1357T>A
|
NP_001373232.1:p.Ser453Thr
|
|
NM_001386304.1:c.1255T>A
|
NP_001373233.1:p.Ser419Thr
|
|
NM_001386305.1:c.1219T>A
|
NP_001373234.1:p.Ser407Thr
|
|
NM_001386306.1:c.1060T>A
|
NP_001373235.1:p.Ser354Thr
|
|