ENST00000267845.8:c.1748G>A
MANE Select
|
ENSP00000267845.3:p.Arg583His
|
|
ENST00000267845.7:c.1748G>A
|
ENSP00000267845.3:p.Arg583His
|
|
ENST00000543581.5:c.1649G>A
|
ENSP00000440252.1:p.Arg550His
|
|
ENST00000559816.1:n.1492G>A
|
|
|
NM_001306146.1:c.1649G>A
|
NP_001293075.1:p.Arg550His
|
|
NM_002112.3:c.1748G>A
|
NP_002103.2:p.Arg583His
|
|
XM_011521479.1:c.1511G>A
|
XP_011519781.1:p.Arg504His
|
|
XM_011521480.1:c.1316G>A
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XP_011519782.1:p.Arg439His
|
|
XM_017022094.1:c.1853G>A
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XP_016877583.1:p.Arg618His
|
|
XM_017022095.1:c.1754G>A
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XP_016877584.1:p.Arg585His
|
|
XM_017022096.1:c.1625G>A
|
XP_016877585.1:p.Arg542His
|
|
XM_017022097.1:c.1616G>A
|
XP_016877586.1:p.Arg539His
|
|
XM_017022098.1:c.1421G>A
|
XP_016877587.1:p.Arg474His
|
|
NM_002112.4:c.1748G>A
MANE Select
|
NP_002103.2:p.Arg583His
|
|
NM_001306146.2:c.1649G>A
|
NP_001293075.1:p.Arg550His
|
|