ENST00000298171.7:c.2060G>A
MANE Select
|
ENSP00000298171.2:p.Arg687Lys
|
|
ENST00000637447.1:c.963G>A
|
|
|
ENST00000298171.6:c.2060G>A
|
ENSP00000298171.2:p.Arg687Lys
|
|
ENST00000541158.6:c.2060G>A
|
ENSP00000441235.2:p.Arg687Lys
|
|
NM_000369.2:c.2060G>A , LRG_523t1:c.2060G>A
|
NP_000360.2:p.Arg687Lys
|
|
XM_005268037.3:c.2060G>A
|
XP_005268094.1:p.Arg687Lys
|
|
XM_011537119.1:c.1781G>A
|
XP_011535421.1:p.Arg594Lys
|
|
XR_245790.3:n.2086+21075C>T
|
|
|
XR_429385.2:n.853+21075C>T
|
|
|
XR_429386.2:n.854+21075C>T
|
|
|
XR_944075.1:n.865+21075C>T
|
|
|
XR_944076.1:n.861+21075C>T
|
|
|
XR_944077.1:n.865+21075C>T
|
|
|
XR_944078.1:n.865+21075C>T
|
|
|
XR_944079.1:n.855+21075C>T
|
|
|
XM_005268037.4:c.2060G>A
|
XP_005268094.1:p.Arg687Lys
|
|
XM_011537119.2:c.1781G>A
|
XP_011535421.1:p.Arg594Lys
|
|
XR_001751021.1:n.2753+21075C>T
|
|
|
XR_001751022.1:n.2753+21075C>T
|
|
|
XR_001751023.1:n.2753+21075C>T
|
|
|
XR_944075.3:n.929+21075C>T
|
|
|
NM_000369.4:c.2060G>A
|
NP_000360.2:p.Arg687Lys
|
|
NM_000369.5:c.2060G>A
MANE Select
|
NP_000360.2:p.Arg687Lys
|
|