ENST00000267845.8:c.1938C>A
MANE Select
|
ENSP00000267845.3:p.Ser646Arg
|
|
ENST00000267845.7:c.1938C>A
|
ENSP00000267845.3:p.Ser646Arg
|
|
ENST00000543581.5:c.1839C>A
|
ENSP00000440252.1:p.Ser613Arg
|
|
ENST00000559816.1:n.1682C>A
|
|
|
NM_001306146.1:c.1839C>A
|
NP_001293075.1:p.Ser613Arg
|
|
NM_002112.3:c.1938C>A
|
NP_002103.2:p.Ser646Arg
|
|
XM_011521479.1:c.1701C>A
|
XP_011519781.1:p.Ser567Arg
|
|
XM_011521480.1:c.1506C>A
|
XP_011519782.1:p.Ser502Arg
|
|
XM_017022094.1:c.2043C>A
|
XP_016877583.1:p.Ser681Arg
|
|
XM_017022095.1:c.1944C>A
|
XP_016877584.1:p.Ser648Arg
|
|
XM_017022096.1:c.1815C>A
|
XP_016877585.1:p.Ser605Arg
|
|
XM_017022097.1:c.1806C>A
|
XP_016877586.1:p.Ser602Arg
|
|
XM_017022098.1:c.1611C>A
|
XP_016877587.1:p.Ser537Arg
|
|
NM_002112.4:c.1938C>A
MANE Select
|
NP_002103.2:p.Ser646Arg
|
|
NM_001306146.2:c.1839C>A
|
NP_001293075.1:p.Ser613Arg
|
|