ENST00000262407.6:c.726C>G
MANE Select
|
ENSP00000262407.5:p.Ile242Met
|
|
ENST00000648408.1:c.157C>G
|
|
|
ENST00000262407.5:c.726C>G
|
ENSP00000262407.5:p.Ile242Met
|
|
ENST00000589645.5:n.177C>G
|
|
|
ENST00000591990.5:n.88C>G
|
|
|
ENST00000592075.5:n.95C>G
|
|
|
ENST00000592226.5:n.39+143C>G
|
|
|
ENST00000592253.5:n.234C>G
|
|
|
ENST00000592944.1:n.408C>G
|
|
|
NM_000419.3:c.726C>G , LRG_479t1:c.726C>G
|
NP_000410.2:p.Ile242Met
|
|
XM_011524749.1:c.726C>G
|
XP_011523051.1:p.Ile242Met
|
|
XM_011524750.1:c.726C>G
|
XP_011523052.1:p.Ile242Met
|
|
NM_000419.4:c.726C>G
|
NP_000410.2:p.Ile242Met
|
|
NM_000419.5:c.726C>G
MANE Select
|
NP_000410.2:p.Ile242Met
|
|