ENST00000367698.4:c.925G>C
MANE Select
|
ENSP00000356671.3:p.Asp309His
|
|
ENST00000367698.3:c.925G>C
|
ENSP00000356671.3:p.Asp309His
|
|
ENST00000487183.1:n.576G>C
|
|
|
ENST00000617423.4:c.559+2084G>C
|
ENSP00000478688.1:n.559+2084G>C
|
|
NM_000488.3:c.925G>C , LRG_577t1:c.925G>C
|
NP_000479.1:p.Asp309His
|
|
XM_005245198.2:c.781G>C
|
XP_005245255.1:p.Asp261His
|
|
NM_001365052.1:c.781G>C
|
NP_001351981.1:p.Asp261His
|
|
NM_000488.4:c.925G>C
MANE Select
|
NP_000479.1:p.Asp309His
|
|
NM_001365052.2:c.781G>C
|
NP_001351981.1:p.Asp261His
|
|
NM_001386302.1:c.1048G>C
|
NP_001373231.1:p.Asp350His
|
|
NM_001386303.1:c.1006G>C
|
NP_001373232.1:p.Asp336His
|
|
NM_001386304.1:c.904G>C
|
NP_001373233.1:p.Asp302His
|
|
NM_001386305.1:c.868G>C
|
NP_001373234.1:p.Asp290His
|
|
NM_001386306.1:c.709G>C
|
NP_001373235.1:p.Asp237His
|
|