ENST00000222248.4:c.1700T>G
MANE Select
|
ENSP00000222248.2:p.Leu567Arg
|
|
ENST00000222248.3:c.1700T>G
|
ENSP00000222248.2:p.Leu567Arg
|
|
NM_000453.2:c.1700T>G
|
NP_000444.1:p.Leu567Arg
|
|
XM_011528192.1:c.1733T>G
|
XP_011526494.1:p.Leu578Arg
|
|
XM_011528193.1:c.1466T>G
|
XP_011526495.1:p.Leu489Arg
|
|
XM_011528194.1:c.1367T>G
|
XP_011526496.1:p.Leu456Arg
|
|
XM_011528192.2:c.1733T>G
|
XP_011526494.1:p.Leu578Arg
|
|
XM_011528193.3:c.1466T>G
|
XP_011526495.1:p.Leu489Arg
|
|
XM_011528194.3:c.1367T>G
|
XP_011526496.1:p.Leu456Arg
|
|
XM_017027158.1:c.1433T>G
|
XP_016882647.1:p.Leu478Arg
|
|
NM_000453.3:c.1700T>G
MANE Select
|
NP_000444.1:p.Leu567Arg
|
|