ENST00000684241.1:n.1226G>C
|
|
|
ENST00000262186.10:c.393G>C
MANE Select
|
ENSP00000262186.5:p.Val131=
|
|
ENST00000262186.9:c.393G>C
|
ENSP00000262186.5:p.Val131=
|
|
ENST00000430723.4:c.216G>C
|
ENSP00000387657.4:p.Val72=
|
|
ENST00000532957.5:n.616G>C
|
|
|
NM_000238.3:c.393G>C , LRG_288t1:c.393G>C
|
NP_000229.1:p.Val131=
|
|
NM_172056.2:c.393G>C , LRG_288t2:c.393G>C
|
NP_742053.1:p.Val131=
|
|
XM_011516185.1:c.93G>C
|
XP_011514487.1:p.Val31=
|
|
XM_011516186.1:c.393G>C
|
XP_011514488.1:p.Val131=
|
|
XM_011516185.2:c.93G>C
|
XP_011514487.1:p.Val31=
|
|
XM_011516186.3:c.393G>C
|
XP_011514488.1:p.Val131=
|
|
XM_017012195.1:c.243G>C
|
XP_016867684.1:p.Val81=
|
|
XM_017012196.1:c.216G>C
|
XP_016867685.1:p.Val72=
|
|
NM_000238.4:c.393G>C
MANE Select
|
NP_000229.1:p.Val131=
|
|