ENST00000267845.8:c.1747C>A
MANE Select
|
ENSP00000267845.3:p.Arg583Ser
|
|
ENST00000267845.7:c.1747C>A
|
ENSP00000267845.3:p.Arg583Ser
|
|
ENST00000543581.5:c.1648C>A
|
ENSP00000440252.1:p.Arg550Ser
|
|
ENST00000559816.1:n.1491C>A
|
|
|
NM_001306146.1:c.1648C>A
|
NP_001293075.1:p.Arg550Ser
|
|
NM_002112.3:c.1747C>A
|
NP_002103.2:p.Arg583Ser
|
|
XM_011521479.1:c.1510C>A
|
XP_011519781.1:p.Arg504Ser
|
|
XM_011521480.1:c.1315C>A
|
XP_011519782.1:p.Arg439Ser
|
|
XM_017022094.1:c.1852C>A
|
XP_016877583.1:p.Arg618Ser
|
|
XM_017022095.1:c.1753C>A
|
XP_016877584.1:p.Arg585Ser
|
|
XM_017022096.1:c.1624C>A
|
XP_016877585.1:p.Arg542Ser
|
|
XM_017022097.1:c.1615C>A
|
XP_016877586.1:p.Arg539Ser
|
|
XM_017022098.1:c.1420C>A
|
XP_016877587.1:p.Arg474Ser
|
|
NM_002112.4:c.1747C>A
MANE Select
|
NP_002103.2:p.Arg583Ser
|
|
NM_001306146.2:c.1648C>A
|
NP_001293075.1:p.Arg550Ser
|
|