ENST00000367698.4:c.1022A>T
MANE Select
|
ENSP00000356671.3:p.Asp341Val
|
|
ENST00000367698.3:c.1022A>T
|
ENSP00000356671.3:p.Asp341Val
|
|
ENST00000617423.4:c.559+2181A>T
|
ENSP00000478688.1:n.559+2181A>T
|
|
NM_000488.3:c.1022A>T , LRG_577t1:c.1022A>T
|
NP_000479.1:p.Asp341Val
|
|
XM_005245198.2:c.878A>T
|
XP_005245255.1:p.Asp293Val
|
|
NM_001365052.1:c.878A>T
|
NP_001351981.1:p.Asp293Val
|
|
NM_000488.4:c.1022A>T
MANE Select
|
NP_000479.1:p.Asp341Val
|
|
NM_001365052.2:c.878A>T
|
NP_001351981.1:p.Asp293Val
|
|
NM_001386302.1:c.1145A>T
|
NP_001373231.1:p.Asp382Val
|
|
NM_001386303.1:c.1103A>T
|
NP_001373232.1:p.Asp368Val
|
|
NM_001386304.1:c.1001A>T
|
NP_001373233.1:p.Asp334Val
|
|
NM_001386305.1:c.965A>T
|
NP_001373234.1:p.Asp322Val
|
|
NM_001386306.1:c.806A>T
|
NP_001373235.1:p.Asp269Val
|
|