ENST00000393716.8:c.442C>G
MANE Select
|
ENSP00000377319.3:p.Arg148Gly
|
|
ENST00000466380.6:c.442C>G
|
ENSP00000420297.2:p.Arg148Gly
|
|
ENST00000337940.4:c.559C>G
|
ENSP00000336528.4:p.Arg187Gly
|
|
ENST00000393716.6:c.442C>G
|
ENSP00000377319.2:p.Arg148Gly
|
|
ENST00000466380.5:c.442C>G
|
ENSP00000420297.1:p.Arg148Gly
|
|
ENST00000493757.1:n.574C>G
|
|
|
NM_003889.3:c.442C>G
|
NP_003880.3:p.Arg148Gly
|
|
NM_022002.2:c.559C>G
|
NP_071285.1:p.Arg187Gly
|
|
NM_033013.2:c.442C>G
|
NP_148934.1:p.Arg148Gly
|
|
NM_003889.4:c.442C>G
MANE Select
|
NP_003880.3:p.Arg148Gly
|
|
NM_022002.3:c.559C>G
|
NP_071285.1:p.Arg187Gly
|
|
NM_033013.3:c.442C>G
|
NP_148934.1:p.Arg148Gly
|
|