ENST00000367698.4:c.844T>A
MANE Select
|
ENSP00000356671.3:p.Ser282Thr
|
|
ENST00000367698.3:c.844T>A
|
ENSP00000356671.3:p.Ser282Thr
|
|
ENST00000487183.1:n.495T>A
|
|
|
ENST00000617423.4:c.559+2003T>A
|
ENSP00000478688.1:n.559+2003T>A
|
|
NM_000488.3:c.844T>A , LRG_577t1:c.844T>A
|
NP_000479.1:p.Ser282Thr
|
|
XM_005245198.2:c.700T>A
|
XP_005245255.1:p.Ser234Thr
|
|
NM_001365052.1:c.700T>A
|
NP_001351981.1:p.Ser234Thr
|
|
NM_000488.4:c.844T>A
MANE Select
|
NP_000479.1:p.Ser282Thr
|
|
NM_001365052.2:c.700T>A
|
NP_001351981.1:p.Ser234Thr
|
|
NM_001386302.1:c.967T>A
|
NP_001373231.1:p.Ser323Thr
|
|
NM_001386303.1:c.925T>A
|
NP_001373232.1:p.Ser309Thr
|
|
NM_001386304.1:c.823T>A
|
NP_001373233.1:p.Ser275Thr
|
|
NM_001386305.1:c.787T>A
|
NP_001373234.1:p.Ser263Thr
|
|
NM_001386306.1:c.628T>A
|
NP_001373235.1:p.Ser210Thr
|
|