ENST00000267845.8:c.1800A>G
MANE Select
|
ENSP00000267845.3:p.Thr600=
|
|
ENST00000267845.7:c.1800A>G
|
ENSP00000267845.3:p.Thr600=
|
|
ENST00000543581.5:c.1701A>G
|
ENSP00000440252.1:p.Thr567=
|
|
ENST00000559816.1:n.1544A>G
|
|
|
NM_001306146.1:c.1701A>G
|
NP_001293075.1:p.Thr567=
|
|
NM_002112.3:c.1800A>G
|
NP_002103.2:p.Thr600=
|
|
XM_011521479.1:c.1563A>G
|
XP_011519781.1:p.Thr521=
|
|
XM_011521480.1:c.1368A>G
|
XP_011519782.1:p.Thr456=
|
|
XM_017022094.1:c.1905A>G
|
XP_016877583.1:p.Thr635=
|
|
XM_017022095.1:c.1806A>G
|
XP_016877584.1:p.Thr602=
|
|
XM_017022096.1:c.1677A>G
|
XP_016877585.1:p.Thr559=
|
|
XM_017022097.1:c.1668A>G
|
XP_016877586.1:p.Thr556=
|
|
XM_017022098.1:c.1473A>G
|
XP_016877587.1:p.Thr491=
|
|
NM_002112.4:c.1800A>G
MANE Select
|
NP_002103.2:p.Thr600=
|
|
NM_001306146.2:c.1701A>G
|
NP_001293075.1:p.Thr567=
|
|