ENST00000267845.8:c.1719G>C
MANE Select
|
ENSP00000267845.3:p.Leu573Phe
|
|
ENST00000267845.7:c.1719G>C
|
ENSP00000267845.3:p.Leu573Phe
|
|
ENST00000543581.5:c.1620G>C
|
ENSP00000440252.1:p.Leu540Phe
|
|
ENST00000559816.1:n.1463G>C
|
|
|
NM_001306146.1:c.1620G>C
|
NP_001293075.1:p.Leu540Phe
|
|
NM_002112.3:c.1719G>C
|
NP_002103.2:p.Leu573Phe
|
|
XM_011521479.1:c.1482G>C
|
XP_011519781.1:p.Leu494Phe
|
|
XM_011521480.1:c.1287G>C
|
XP_011519782.1:p.Leu429Phe
|
|
XM_017022094.1:c.1824G>C
|
XP_016877583.1:p.Leu608Phe
|
|
XM_017022095.1:c.1725G>C
|
XP_016877584.1:p.Leu575Phe
|
|
XM_017022096.1:c.1596G>C
|
XP_016877585.1:p.Leu532Phe
|
|
XM_017022097.1:c.1587G>C
|
XP_016877586.1:p.Leu529Phe
|
|
XM_017022098.1:c.1392G>C
|
XP_016877587.1:p.Leu464Phe
|
|
NM_002112.4:c.1719G>C
MANE Select
|
NP_002103.2:p.Leu573Phe
|
|
NM_001306146.2:c.1620G>C
|
NP_001293075.1:p.Leu540Phe
|
|