ENST00000684241.1:n.1913A>T
|
|
|
ENST00000262186.10:c.1080A>T
MANE Select
|
ENSP00000262186.5:p.Ala360=
|
|
ENST00000262186.9:c.1080A>T
|
ENSP00000262186.5:p.Ala360=
|
|
ENST00000430723.4:c.732A>T
|
ENSP00000387657.4:p.Ala244=
|
|
ENST00000532957.5:n.1303A>T
|
|
|
NM_000238.3:c.1080A>T , LRG_288t1:c.1080A>T
|
NP_000229.1:p.Ala360=
|
|
NM_172056.2:c.1080A>T , LRG_288t2:c.1080A>T
|
NP_742053.1:p.Ala360=
|
|
XM_011516185.1:c.780A>T
|
XP_011514487.1:p.Ala260=
|
|
XM_011516186.1:c.1080A>T
|
XP_011514488.1:p.Ala360=
|
|
XM_011516185.2:c.780A>T
|
XP_011514487.1:p.Ala260=
|
|
XM_011516186.3:c.1080A>T
|
XP_011514488.1:p.Ala360=
|
|
XM_017012195.1:c.930A>T
|
XP_016867684.1:p.Ala310=
|
|
XM_017012196.1:c.903A>T
|
XP_016867685.1:p.Ala301=
|
|
NM_000238.4:c.1080A>T
MANE Select
|
NP_000229.1:p.Ala360=
|
|