ENST00000267845.8:c.1705C>G
MANE Select
|
ENSP00000267845.3:p.Leu569Val
|
|
ENST00000267845.7:c.1705C>G
|
ENSP00000267845.3:p.Leu569Val
|
|
ENST00000543581.5:c.1606C>G
|
ENSP00000440252.1:p.Leu536Val
|
|
ENST00000559816.1:n.1449C>G
|
|
|
NM_001306146.1:c.1606C>G
|
NP_001293075.1:p.Leu536Val
|
|
NM_002112.3:c.1705C>G
|
NP_002103.2:p.Leu569Val
|
|
XM_011521479.1:c.1468C>G
|
XP_011519781.1:p.Leu490Val
|
|
XM_011521480.1:c.1273C>G
|
XP_011519782.1:p.Leu425Val
|
|
XM_017022094.1:c.1810C>G
|
XP_016877583.1:p.Leu604Val
|
|
XM_017022095.1:c.1711C>G
|
XP_016877584.1:p.Leu571Val
|
|
XM_017022096.1:c.1582C>G
|
XP_016877585.1:p.Leu528Val
|
|
XM_017022097.1:c.1573C>G
|
XP_016877586.1:p.Leu525Val
|
|
XM_017022098.1:c.1378C>G
|
XP_016877587.1:p.Leu460Val
|
|
NM_002112.4:c.1705C>G
MANE Select
|
NP_002103.2:p.Leu569Val
|
|
NM_001306146.2:c.1606C>G
|
NP_001293075.1:p.Leu536Val
|
|