ENST00000684241.1:n.1901T>C
|
|
|
ENST00000262186.10:c.1068T>C
MANE Select
|
ENSP00000262186.5:p.Arg356=
|
|
ENST00000262186.9:c.1068T>C
|
ENSP00000262186.5:p.Arg356=
|
|
ENST00000430723.4:c.720T>C
|
ENSP00000387657.4:p.Arg240=
|
|
ENST00000532957.5:n.1291T>C
|
|
|
NM_000238.3:c.1068T>C , LRG_288t1:c.1068T>C
|
NP_000229.1:p.Arg356=
|
|
NM_172056.2:c.1068T>C , LRG_288t2:c.1068T>C
|
NP_742053.1:p.Arg356=
|
|
XM_011516185.1:c.768T>C
|
XP_011514487.1:p.Arg256=
|
|
XM_011516186.1:c.1068T>C
|
XP_011514488.1:p.Arg356=
|
|
XM_011516185.2:c.768T>C
|
XP_011514487.1:p.Arg256=
|
|
XM_011516186.3:c.1068T>C
|
XP_011514488.1:p.Arg356=
|
|
XM_017012195.1:c.918T>C
|
XP_016867684.1:p.Arg306=
|
|
XM_017012196.1:c.891T>C
|
XP_016867685.1:p.Arg297=
|
|
NM_000238.4:c.1068T>C
MANE Select
|
NP_000229.1:p.Arg356=
|
|