ENST00000267845.8:c.1956G>C
MANE Select
|
ENSP00000267845.3:p.Gln652His
|
|
ENST00000267845.7:c.1956G>C
|
ENSP00000267845.3:p.Gln652His
|
|
ENST00000543581.5:c.1857G>C
|
ENSP00000440252.1:p.Gln619His
|
|
ENST00000559816.1:n.1700G>C
|
|
|
NM_001306146.1:c.1857G>C
|
NP_001293075.1:p.Gln619His
|
|
NM_002112.3:c.1956G>C
|
NP_002103.2:p.Gln652His
|
|
XM_011521479.1:c.1719G>C
|
XP_011519781.1:p.Gln573His
|
|
XM_011521480.1:c.1524G>C
|
XP_011519782.1:p.Gln508His
|
|
XM_017022094.1:c.2061G>C
|
XP_016877583.1:p.Gln687His
|
|
XM_017022095.1:c.1962G>C
|
XP_016877584.1:p.Gln654His
|
|
XM_017022096.1:c.1833G>C
|
XP_016877585.1:p.Gln611His
|
|
XM_017022097.1:c.1824G>C
|
XP_016877586.1:p.Gln608His
|
|
XM_017022098.1:c.1629G>C
|
XP_016877587.1:p.Gln543His
|
|
NM_002112.4:c.1956G>C
MANE Select
|
NP_002103.2:p.Gln652His
|
|
NM_001306146.2:c.1857G>C
|
NP_001293075.1:p.Gln619His
|
|