ENST00000248633.9:c.2621G>C
MANE Select
|
ENSP00000248633.4:p.Arg874Thr
|
|
ENST00000248633.8:c.2621G>C
|
ENSP00000248633.4:p.Arg874Thr
|
|
ENST00000428214.5:c.2450G>C
|
ENSP00000394413.1:p.Arg817Thr
|
|
ENST00000438045.5:c.1655G>C
|
ENSP00000410438.1:p.Arg552Thr
|
|
ENST00000484913.5:n.2660G>C
|
|
|
ENST00000496420.5:n.2513G>C
|
|
|
NM_000466.2:c.2621G>C
|
NP_000457.1:p.Arg874Thr
|
|
NM_001282677.1:c.2450G>C
|
NP_001269606.1:p.Arg817Thr
|
|
NM_001282678.1:c.1997G>C
|
NP_001269607.1:p.Arg666Thr
|
|
XM_005250433.3:c.872G>C
|
XP_005250490.1:p.Arg291Thr
|
|
XR_242246.3:n.2717G>C
|
|
|
XM_017012319.2:c.872G>C
|
XP_016867808.1:p.Arg291Thr
|
|
XR_001744808.2:n.1648G>C
|
|
|
XR_242246.5:n.2668G>C
|
|
|
NM_000466.3:c.2621G>C
MANE Select
|
NP_000457.1:p.Arg874Thr
|
|
NM_001282677.2:c.2450G>C
|
NP_001269606.1:p.Arg817Thr
|
|
NM_001282678.2:c.1997G>C
|
NP_001269607.1:p.Arg666Thr
|
|