ENST00000461280.2:n.617C=
|
|
|
ENST00000684116.1:n.212C=
|
|
|
ENST00000684241.1:n.2152C=
|
|
|
ENST00000262186.10:c.1319C=
MANE Select
|
ENSP00000262186.5:p.Pro440=
|
|
ENST00000330883.9:c.299C=
|
ENSP00000328531.4:p.Pro100=
|
|
ENST00000262186.9:c.1319C=
|
ENSP00000262186.5:p.Pro440=
|
|
ENST00000330883.8:c.299C=
|
ENSP00000328531.4:p.Pro100=
|
|
ENST00000430723.4:c.971C=
|
ENSP00000387657.4:p.Pro324=
|
|
ENST00000461280.1:n.606C=
|
|
|
ENST00000473610.5:n.624C=
|
|
|
ENST00000532957.5:n.1542C=
|
|
|
NM_000238.3:c.1319C= , LRG_288t1:c.1319C=
|
NP_000229.1:p.Pro440=
|
|
NM_001204798.1:c.299C=
|
NP_001191727.1:p.Pro100=
|
|
NM_172056.2:c.1319C= , LRG_288t2:c.1319C=
|
NP_742053.1:p.Pro440=
|
|
NM_172057.2:c.299C= , LRG_288t3:c.299C=
|
NP_742054.1:p.Pro100=
|
|
XM_011516185.1:c.1019C=
|
XP_011514487.1:p.Pro340=
|
|
XM_011516186.1:c.1319C=
|
XP_011514488.1:p.Pro440=
|
|
XM_011516185.2:c.1019C=
|
XP_011514487.1:p.Pro340=
|
|
XM_011516186.3:c.1319C=
|
XP_011514488.1:p.Pro440=
|
|
XM_017012195.1:c.1169C=
|
XP_016867684.1:p.Pro390=
|
|
XM_017012196.1:c.1142C=
|
XP_016867685.1:p.Pro381=
|
|
NM_000238.4:c.1319C=
MANE Select
|
NP_000229.1:p.Pro440=
|
|
NM_001204798.2:c.299C=
|
NP_001191727.1:p.Pro100=
|
|
NM_172057.3:c.299C=
|
NP_742054.1:p.Pro100=
|
|