ENST00000450565.8:c.176C>G
MANE Select
|
ENSP00000411658.3:p.Pro59Arg
|
|
ENST00000269200.5:n.174C>G
|
|
|
ENST00000450565.7:c.176C>G
|
ENSP00000411658.3:p.Pro59Arg
|
|
ENST00000579794.1:c.176C>G
|
ENSP00000462647.1:p.Pro59Arg
|
|
NM_001099733.1:c.176C>G
|
NP_001093203.1:p.Pro59Arg
|
|
NM_001117.4:c.176C>G
|
NP_001108.2:p.Pro59Arg
|
|
XM_005258081.2:c.659C>G
|
XP_005258138.1:p.Pro220Arg
|
|
XM_005258081.4:c.593C>G
|
XP_005258138.2:p.Pro198Arg
|
|
NM_001099733.2:c.176C>G
MANE Select
|
NP_001093203.1:p.Pro59Arg
|
|
NM_001117.5:c.176C>G
|
NP_001108.2:p.Pro59Arg
|
|