ENST00000461280.2:n.1122G=
|
|
|
ENST00000684241.1:n.2657G=
|
|
|
ENST00000262186.10:c.1824G=
MANE Select
|
ENSP00000262186.5:p.Lys608=
|
|
ENST00000330883.9:c.804G=
|
ENSP00000328531.4:p.Lys268=
|
|
ENST00000262186.9:c.1824G=
|
ENSP00000262186.5:p.Lys608=
|
|
ENST00000330883.8:c.804G=
|
ENSP00000328531.4:p.Lys268=
|
|
ENST00000430723.4:c.1476G=
|
ENSP00000387657.4:p.Lys492=
|
|
ENST00000461280.1:n.1111G=
|
|
|
ENST00000473610.5:n.1129G=
|
|
|
ENST00000532957.5:n.2047G=
|
|
|
NM_000238.3:c.1824G= , LRG_288t1:c.1824G=
|
NP_000229.1:p.Lys608=
|
|
NM_001204798.1:c.804G=
|
NP_001191727.1:p.Lys268=
|
|
NM_172056.2:c.1824G= , LRG_288t2:c.1824G=
|
NP_742053.1:p.Lys608=
|
|
NM_172057.2:c.804G= , LRG_288t3:c.804G=
|
NP_742054.1:p.Lys268=
|
|
XM_011516185.1:c.1524G=
|
XP_011514487.1:p.Lys508=
|
|
XM_011516186.1:c.1824G=
|
XP_011514488.1:p.Lys608=
|
|
XM_011516185.2:c.1524G=
|
XP_011514487.1:p.Lys508=
|
|
XM_011516186.3:c.1824G=
|
XP_011514488.1:p.Lys608=
|
|
XM_017012195.1:c.1674G=
|
XP_016867684.1:p.Lys558=
|
|
XM_017012196.1:c.1647G=
|
XP_016867685.1:p.Lys549=
|
|
NM_000238.4:c.1824G=
MANE Select
|
NP_000229.1:p.Lys608=
|
|
NM_001204798.2:c.804G=
|
NP_001191727.1:p.Lys268=
|
|
NM_172057.3:c.804G=
|
NP_742054.1:p.Lys268=
|
|