ENST00000313468.10:c.567C>A
MANE Select
|
ENSP00000315774.5:p.Leu189=
|
|
ENST00000313468.9:c.567C>A
|
ENSP00000315774.5:p.Leu189=
|
|
ENST00000524810.5:c.499C>A
|
|
|
ENST00000526446.5:c.*622C>A
|
ENSP00000433645.1:n.*622C>A
|
|
ENST00000528492.1:c.129C>A
|
ENSP00000432848.1:p.Leu43=
|
|
ENST00000531282.1:n.419C>A
|
|
|
NM_002496.3:c.567C>A
|
NP_002487.1:p.Leu189=
|
|
XM_005274013.1:c.567C>A
|
XP_005274070.1:p.Leu189=
|
|
XM_005274014.1:c.567C>A
|
XP_005274071.1:p.Leu189=
|
|
XM_005274015.1:c.447C>A
|
XP_005274072.1:p.Leu149=
|
|
XM_011545053.1:c.567C>A
|
XP_011543355.1:p.Leu189=
|
|
NM_002496.4:c.567C>A
MANE Select
|
NP_002487.1:p.Leu189=
|
|