ENST00000267845.8:c.1675G>C
MANE Select
|
ENSP00000267845.3:p.Asp559His
|
|
ENST00000267845.7:c.1675G>C
|
ENSP00000267845.3:p.Asp559His
|
|
ENST00000543581.5:c.1576G>C
|
ENSP00000440252.1:p.Asp526His
|
|
ENST00000559816.1:n.1419G>C
|
|
|
NM_001306146.1:c.1576G>C
|
NP_001293075.1:p.Asp526His
|
|
NM_002112.3:c.1675G>C
|
NP_002103.2:p.Asp559His
|
|
XM_011521479.1:c.1438G>C
|
XP_011519781.1:p.Asp480His
|
|
XM_011521480.1:c.1243G>C
|
XP_011519782.1:p.Asp415His
|
|
XM_017022094.1:c.1780G>C
|
XP_016877583.1:p.Asp594His
|
|
XM_017022095.1:c.1681G>C
|
XP_016877584.1:p.Asp561His
|
|
XM_017022096.1:c.1552G>C
|
XP_016877585.1:p.Asp518His
|
|
XM_017022097.1:c.1543G>C
|
XP_016877586.1:p.Asp515His
|
|
XM_017022098.1:c.1348G>C
|
XP_016877587.1:p.Asp450His
|
|
NM_002112.4:c.1675G>C
MANE Select
|
NP_002103.2:p.Asp559His
|
|
NM_001306146.2:c.1576G>C
|
NP_001293075.1:p.Asp526His
|
|