ENST00000267845.8:c.1754T>A
MANE Select
|
ENSP00000267845.3:p.Leu585His
|
|
ENST00000267845.7:c.1754T>A
|
ENSP00000267845.3:p.Leu585His
|
|
ENST00000543581.5:c.1655T>A
|
ENSP00000440252.1:p.Leu552His
|
|
ENST00000559816.1:n.1498T>A
|
|
|
NM_001306146.1:c.1655T>A
|
NP_001293075.1:p.Leu552His
|
|
NM_002112.3:c.1754T>A
|
NP_002103.2:p.Leu585His
|
|
XM_011521479.1:c.1517T>A
|
XP_011519781.1:p.Leu506His
|
|
XM_011521480.1:c.1322T>A
|
XP_011519782.1:p.Leu441His
|
|
XM_017022094.1:c.1859T>A
|
XP_016877583.1:p.Leu620His
|
|
XM_017022095.1:c.1760T>A
|
XP_016877584.1:p.Leu587His
|
|
XM_017022096.1:c.1631T>A
|
XP_016877585.1:p.Leu544His
|
|
XM_017022097.1:c.1622T>A
|
XP_016877586.1:p.Leu541His
|
|
XM_017022098.1:c.1427T>A
|
XP_016877587.1:p.Leu476His
|
|
NM_002112.4:c.1754T>A
MANE Select
|
NP_002103.2:p.Leu585His
|
|
NM_001306146.2:c.1655T>A
|
NP_001293075.1:p.Leu552His
|
|