ENST00000313468.10:c.339C>A
MANE Select
|
ENSP00000315774.5:p.Ala113=
|
|
ENST00000313468.9:c.339C>A
|
ENSP00000315774.5:p.Ala113=
|
|
ENST00000432321.6:n.456C>A
|
|
|
ENST00000453471.6:c.339C>A
|
ENSP00000403972.2:p.Ala113=
|
|
ENST00000524810.5:c.110C>A
|
|
|
ENST00000525419.5:c.285C>A
|
ENSP00000433521.1:p.Ala95=
|
|
ENST00000526339.5:c.339C>A
|
ENSP00000436287.1:p.Ala113=
|
|
ENST00000526446.5:c.*394C>A
|
ENSP00000433645.1:n.*394C>A
|
|
ENST00000528492.1:c.-67+2517C>A
|
ENSP00000432848.1:n.-67+2517C>A
|
|
ENST00000529645.1:c.517C>A
|
ENSP00000431293.1:n.517C>A
|
|
ENST00000532399.1:n.1044C>A
|
|
|
NM_002496.3:c.339C>A
|
NP_002487.1:p.Ala113=
|
|
XM_005274013.1:c.339C>A
|
XP_005274070.1:p.Ala113=
|
|
XM_005274014.1:c.339C>A
|
XP_005274071.1:p.Ala113=
|
|
XM_005274015.1:c.219C>A
|
XP_005274072.1:p.Ala73=
|
|
XM_011545053.1:c.339C>A
|
XP_011543355.1:p.Ala113=
|
|
NM_002496.4:c.339C>A
MANE Select
|
NP_002487.1:p.Ala113=
|
|