ENST00000684241.1:n.1676C=
|
|
|
ENST00000262186.10:c.843C=
MANE Select
|
ENSP00000262186.5:p.Arg281=
|
|
ENST00000262186.9:c.843C=
|
ENSP00000262186.5:p.Arg281=
|
|
ENST00000430723.4:c.495C=
|
ENSP00000387657.4:p.Arg165=
|
|
ENST00000532957.5:n.1066C=
|
|
|
NM_000238.3:c.843C= , LRG_288t1:c.843C=
|
NP_000229.1:p.Arg281=
|
|
NM_172056.2:c.843C= , LRG_288t2:c.843C=
|
NP_742053.1:p.Arg281=
|
|
XM_011516185.1:c.543C=
|
XP_011514487.1:p.Arg181=
|
|
XM_011516186.1:c.843C=
|
XP_011514488.1:p.Arg281=
|
|
XM_011516185.2:c.543C=
|
XP_011514487.1:p.Arg181=
|
|
XM_011516186.3:c.843C=
|
XP_011514488.1:p.Arg281=
|
|
XM_017012195.1:c.693C=
|
XP_016867684.1:p.Arg231=
|
|
XM_017012196.1:c.666C=
|
XP_016867685.1:p.Arg222=
|
|
NM_000238.4:c.843C=
MANE Select
|
NP_000229.1:p.Arg281=
|
|