ENST00000393958.7:c.2493G>A
|
ENSP00000377530.2:p.Val831=
|
|
ENST00000393960.7:c.2493G>A
MANE Select
|
ENSP00000377532.1:p.Val831=
|
|
ENST00000525476.2:n.290-380G>A
|
|
|
ENST00000528224.2:c.*502G>A
|
ENSP00000498317.1:n.*502G>A
|
|
ENST00000529047.6:c.2493G>A
|
ENSP00000435905.2:p.Val831=
|
|
ENST00000651036.1:c.2493G>A
|
ENSP00000498406.1:p.Val831=
|
|
ENST00000651469.1:c.*969G>A
|
ENSP00000498712.1:n.*969G>A
|
|
ENST00000651854.1:c.2493G>A
|
ENSP00000498994.1:p.Val831=
|
|
ENST00000652125.1:c.2493G>A
|
ENSP00000498302.1:p.Val831=
|
|
ENST00000393955.6:c.2493G>A
|
ENSP00000377527.2:p.Val831=
|
|
ENST00000393958.6:c.2493G>A
|
ENSP00000377530.2:p.Val831=
|
|
ENST00000393960.5:c.2493G>A
|
ENSP00000377532.1:p.Val831=
|
|
NM_000920.3:c.2493G>A
|
NP_000911.2:p.Val831=
|
|
NM_001040716.1:c.2493G>A
|
NP_001035806.1:p.Val831=
|
|
NM_022172.2:c.2493G>A
|
NP_071504.2:p.Val831=
|
|
XM_005274031.3:c.2493G>A
|
XP_005274088.1:p.Val831=
|
|
XM_005274032.3:c.2493G>A
|
XP_005274089.1:p.Val831=
|
|
XM_006718577.2:c.2493G>A
|
XP_006718640.1:p.Val831=
|
|
XM_006718578.2:c.2493G>A
|
XP_006718641.1:p.Val831=
|
|
XM_006718579.2:c.972G>A
|
XP_006718642.1:p.Val324=
|
|
XM_011545085.1:c.2493G>A
|
XP_011543387.1:p.Val831=
|
|
XM_011545086.1:c.2493G>A
|
XP_011543388.1:p.Val831=
|
|
XM_011545087.1:c.1197G>A
|
XP_011543389.1:p.Val399=
|
|
XM_011545088.1:c.1128G>A
|
XP_011543390.1:p.Val376=
|
|
XM_005274031.4:c.2493G>A
|
XP_005274088.1:p.Val831=
|
|
XM_005274032.4:c.2493G>A
|
XP_005274089.1:p.Val831=
|
|
XM_006718578.3:c.2493G>A
|
XP_006718641.1:p.Val831=
|
|
XM_006718579.3:c.972G>A
|
XP_006718642.1:p.Val324=
|
|
XM_011545086.2:c.2493G>A
|
XP_011543388.1:p.Val831=
|
|
XM_011545087.2:c.1197G>A
|
XP_011543389.1:p.Val399=
|
|
XM_017017868.1:c.2493G>A
|
XP_016873357.1:p.Val831=
|
|
XM_017017869.1:c.2493G>A
|
XP_016873358.1:p.Val831=
|
|
XM_017017870.1:c.2493G>A
|
XP_016873359.1:p.Val831=
|
|
XM_017017871.1:c.2493G>A
|
XP_016873360.1:p.Val831=
|
|
XM_017017872.2:c.2493G>A
|
XP_016873361.1:p.Val831=
|
|
NM_000920.4:c.2493G>A
|
NP_000911.2:p.Val831=
|
|
NM_001040716.2:c.2493G>A
MANE Select
|
NP_001035806.1:p.Val831=
|
|
NM_022172.3:c.2493G>A
|
NP_071504.2:p.Val831=
|
|