ENST00000684241.1:n.1685G>T
|
|
|
ENST00000262186.10:c.852G>T
MANE Select
|
ENSP00000262186.5:p.Ser284=
|
|
ENST00000262186.9:c.852G>T
|
ENSP00000262186.5:p.Ser284=
|
|
ENST00000430723.4:c.504G>T
|
ENSP00000387657.4:p.Ser168=
|
|
ENST00000532957.5:n.1075G>T
|
|
|
NM_000238.3:c.852G>T , LRG_288t1:c.852G>T
|
NP_000229.1:p.Ser284=
|
|
NM_172056.2:c.852G>T , LRG_288t2:c.852G>T
|
NP_742053.1:p.Ser284=
|
|
XM_011516185.1:c.552G>T
|
XP_011514487.1:p.Ser184=
|
|
XM_011516186.1:c.852G>T
|
XP_011514488.1:p.Ser284=
|
|
XM_011516185.2:c.552G>T
|
XP_011514487.1:p.Ser184=
|
|
XM_011516186.3:c.852G>T
|
XP_011514488.1:p.Ser284=
|
|
XM_017012195.1:c.702G>T
|
XP_016867684.1:p.Ser234=
|
|
XM_017012196.1:c.675G>T
|
XP_016867685.1:p.Ser225=
|
|
NM_000238.4:c.852G>T
MANE Select
|
NP_000229.1:p.Ser284=
|
|