ENST00000267845.8:c.1851G>T
MANE Select
|
ENSP00000267845.3:p.Arg617Ser
|
|
ENST00000267845.7:c.1851G>T
|
ENSP00000267845.3:p.Arg617Ser
|
|
ENST00000543581.5:c.1752G>T
|
ENSP00000440252.1:p.Arg584Ser
|
|
ENST00000559816.1:n.1595G>T
|
|
|
NM_001306146.1:c.1752G>T
|
NP_001293075.1:p.Arg584Ser
|
|
NM_002112.3:c.1851G>T
|
NP_002103.2:p.Arg617Ser
|
|
XM_011521479.1:c.1614G>T
|
XP_011519781.1:p.Arg538Ser
|
|
XM_011521480.1:c.1419G>T
|
XP_011519782.1:p.Arg473Ser
|
|
XM_017022094.1:c.1956G>T
|
XP_016877583.1:p.Arg652Ser
|
|
XM_017022095.1:c.1857G>T
|
XP_016877584.1:p.Arg619Ser
|
|
XM_017022096.1:c.1728G>T
|
XP_016877585.1:p.Arg576Ser
|
|
XM_017022097.1:c.1719G>T
|
XP_016877586.1:p.Arg573Ser
|
|
XM_017022098.1:c.1524G>T
|
XP_016877587.1:p.Arg508Ser
|
|
NM_002112.4:c.1851G>T
MANE Select
|
NP_002103.2:p.Arg617Ser
|
|
NM_001306146.2:c.1752G>T
|
NP_001293075.1:p.Arg584Ser
|
|