ENST00000267845.8:c.1893A>G
MANE Select
|
ENSP00000267845.3:p.Lys631=
|
|
ENST00000267845.7:c.1893A>G
|
ENSP00000267845.3:p.Lys631=
|
|
ENST00000543581.5:c.1794A>G
|
ENSP00000440252.1:p.Lys598=
|
|
ENST00000559816.1:n.1637A>G
|
|
|
NM_001306146.1:c.1794A>G
|
NP_001293075.1:p.Lys598=
|
|
NM_002112.3:c.1893A>G
|
NP_002103.2:p.Lys631=
|
|
XM_011521479.1:c.1656A>G
|
XP_011519781.1:p.Lys552=
|
|
XM_011521480.1:c.1461A>G
|
XP_011519782.1:p.Lys487=
|
|
XM_017022094.1:c.1998A>G
|
XP_016877583.1:p.Lys666=
|
|
XM_017022095.1:c.1899A>G
|
XP_016877584.1:p.Lys633=
|
|
XM_017022096.1:c.1770A>G
|
XP_016877585.1:p.Lys590=
|
|
XM_017022097.1:c.1761A>G
|
XP_016877586.1:p.Lys587=
|
|
XM_017022098.1:c.1566A>G
|
XP_016877587.1:p.Lys522=
|
|
NM_002112.4:c.1893A>G
MANE Select
|
NP_002103.2:p.Lys631=
|
|
NM_001306146.2:c.1794A>G
|
NP_001293075.1:p.Lys598=
|
|