ENST00000267845.8:c.1718T>G
MANE Select
|
ENSP00000267845.3:p.Leu573Trp
|
|
ENST00000267845.7:c.1718T>G
|
ENSP00000267845.3:p.Leu573Trp
|
|
ENST00000543581.5:c.1619T>G
|
ENSP00000440252.1:p.Leu540Trp
|
|
ENST00000559816.1:n.1462T>G
|
|
|
NM_001306146.1:c.1619T>G
|
NP_001293075.1:p.Leu540Trp
|
|
NM_002112.3:c.1718T>G
|
NP_002103.2:p.Leu573Trp
|
|
XM_011521479.1:c.1481T>G
|
XP_011519781.1:p.Leu494Trp
|
|
XM_011521480.1:c.1286T>G
|
XP_011519782.1:p.Leu429Trp
|
|
XM_017022094.1:c.1823T>G
|
XP_016877583.1:p.Leu608Trp
|
|
XM_017022095.1:c.1724T>G
|
XP_016877584.1:p.Leu575Trp
|
|
XM_017022096.1:c.1595T>G
|
XP_016877585.1:p.Leu532Trp
|
|
XM_017022097.1:c.1586T>G
|
XP_016877586.1:p.Leu529Trp
|
|
XM_017022098.1:c.1391T>G
|
XP_016877587.1:p.Leu464Trp
|
|
NM_002112.4:c.1718T>G
MANE Select
|
NP_002103.2:p.Leu573Trp
|
|
NM_001306146.2:c.1619T>G
|
NP_001293075.1:p.Leu540Trp
|
|