ENST00000461280.2:n.1581A>C
|
|
|
ENST00000684241.1:n.3116A>C
|
|
|
ENST00000262186.10:c.2283A>C
MANE Select
|
ENSP00000262186.5:p.Thr761=
|
|
ENST00000330883.9:c.1263A>C
|
ENSP00000328531.4:p.Thr421=
|
|
ENST00000262186.9:c.2283A>C
|
ENSP00000262186.5:p.Thr761=
|
|
ENST00000330883.8:c.1263A>C
|
ENSP00000328531.4:p.Thr421=
|
|
ENST00000430723.4:c.1935A>C
|
ENSP00000387657.4:p.Thr645=
|
|
ENST00000461280.1:n.1570A>C
|
|
|
ENST00000473610.5:n.1915A>C
|
|
|
ENST00000532957.5:n.2506A>C
|
|
|
NM_000238.3:c.2283A>C , LRG_288t1:c.2283A>C
|
NP_000229.1:p.Thr761=
|
|
NM_001204798.1:c.1263A>C
|
NP_001191727.1:p.Thr421=
|
|
NM_172056.2:c.2283A>C , LRG_288t2:c.2283A>C
|
NP_742053.1:p.Thr761=
|
|
NM_172057.2:c.1263A>C , LRG_288t3:c.1263A>C
|
NP_742054.1:p.Thr421=
|
|
XM_011516185.1:c.1983A>C
|
XP_011514487.1:p.Thr661=
|
|
XM_011516186.1:c.2283A>C
|
XP_011514488.1:p.Thr761=
|
|
XM_011516185.2:c.1983A>C
|
XP_011514487.1:p.Thr661=
|
|
XM_011516186.3:c.2283A>C
|
XP_011514488.1:p.Thr761=
|
|
XM_017012195.1:c.2133A>C
|
XP_016867684.1:p.Thr711=
|
|
XM_017012196.1:c.2106A>C
|
XP_016867685.1:p.Thr702=
|
|
NM_000238.4:c.2283A>C
MANE Select
|
NP_000229.1:p.Thr761=
|
|
NM_001204798.2:c.1263A>C
|
NP_001191727.1:p.Thr421=
|
|
NM_172057.3:c.1263A>C
|
NP_742054.1:p.Thr421=
|
|