ENST00000684241.1:n.3530G>T
|
|
|
ENST00000262186.10:c.2697G>T
MANE Select
|
ENSP00000262186.5:p.Thr899=
|
|
ENST00000330883.9:c.1677G>T
|
ENSP00000328531.4:p.Thr559=
|
|
ENST00000262186.9:c.2697G>T
|
ENSP00000262186.5:p.Thr899=
|
|
ENST00000330883.8:c.1677G>T
|
ENSP00000328531.4:p.Thr559=
|
|
NM_000238.3:c.2697G>T , LRG_288t1:c.2697G>T
|
NP_000229.1:p.Thr899=
|
|
NM_172057.2:c.1677G>T , LRG_288t3:c.1677G>T
|
NP_742054.1:p.Thr559=
|
|
XM_011516185.1:c.2397G>T
|
XP_011514487.1:p.Thr799=
|
|
XM_011516186.1:c.2693-183G>T
|
XP_011514488.1:n.2693-183G>T
|
|
XM_011516185.2:c.2397G>T
|
XP_011514487.1:p.Thr799=
|
|
XM_011516186.3:c.2693-183G>T
|
XP_011514488.1:n.2693-183G>T
|
|
XM_017012195.1:c.2547G>T
|
XP_016867684.1:p.Thr849=
|
|
XM_017012196.1:c.2520G>T
|
XP_016867685.1:p.Thr840=
|
|
NM_000238.4:c.2697G>T
MANE Select
|
NP_000229.1:p.Thr899=
|
|
NM_172057.3:c.1677G>T
|
NP_742054.1:p.Thr559=
|
|