|
ENST00000367698.4:c.1249A>T
MANE Select
|
ENSP00000356671.3:p.Ser417Cys
|
|
|
ENST00000367698.3:c.1249A>T
|
ENSP00000356671.3:p.Ser417Cys
|
|
|
ENST00000617423.4:c.634A>T
|
ENSP00000478688.1:p.Ser212Cys
|
|
|
NM_000488.3:c.1249A>T , LRG_577t1:c.1249A>T
|
NP_000479.1:p.Ser417Cys
|
|
|
XM_005245198.2:c.1105A>T
|
XP_005245255.1:p.Ser369Cys
|
|
|
NM_001365052.1:c.1105A>T
|
NP_001351981.1:p.Ser369Cys
|
|
|
NM_000488.4:c.1249A>T
MANE Select
|
NP_000479.1:p.Ser417Cys
|
|
|
NM_001365052.2:c.1105A>T
|
NP_001351981.1:p.Ser369Cys
|
|
|
NM_001386302.1:c.1372A>T
|
NP_001373231.1:p.Ser458Cys
|
|
|
NM_001386303.1:c.1330A>T
|
NP_001373232.1:p.Ser444Cys
|
|
|
NM_001386304.1:c.1228A>T
|
NP_001373233.1:p.Ser410Cys
|
|
|
NM_001386305.1:c.1192A>T
|
NP_001373234.1:p.Ser398Cys
|
|
|
NM_001386306.1:c.1033A>T
|
NP_001373235.1:p.Ser345Cys
|
|
