ENST00000622290.5:c.3693G>A
|
ENSP00000483331.2:p.Val1231=
|
|
ENST00000205557.12:c.3693G>A
MANE Select
|
ENSP00000205557.7:p.Val1231=
|
|
ENST00000640696.1:c.507G>A
|
ENSP00000492197.1:p.Val169=
|
|
ENST00000205557.11:c.3693G>A
|
ENSP00000205557.7:p.Val1231=
|
|
ENST00000456970.6:c.3318G>A
|
ENSP00000405002.2:n.3318G>A
|
|
ENST00000622290.4:c.*902G>A
|
ENSP00000483331.1:n.*902G>A
|
|
NM_001171.5:c.3693G>A
|
NP_001162.4:p.Val1231=
|
|
XM_011522479.1:c.3660G>A
|
XP_011520781.1:p.Val1220=
|
|
XM_011522480.1:c.3351G>A
|
XP_011520782.1:p.Val1117=
|
|
XM_011522481.1:c.3351G>A
|
XP_011520783.1:p.Val1117=
|
|
XR_932836.1:n.3928G>A
|
|
|
XR_932837.1:n.3729G>A
|
|
|
XR_932838.1:n.3729G>A
|
|
|
XR_933134.1:n.539-257C>T
|
|
|
NM_001351800.1:c.3351G>A
|
NP_001338729.1:p.Val1117=
|
|
NR_147784.1:n.3355G>A
|
|
|
XM_011522479.2:c.3660G>A
|
XP_011520781.1:p.Val1220=
|
|
XM_011522481.3:c.3351G>A
|
XP_011520783.1:p.Val1117=
|
|
XM_017023212.1:c.3525G>A
|
XP_016878701.1:p.Val1175=
|
|
XM_024450261.1:c.3729G>A
|
XP_024306029.1:p.Val1243=
|
|
XR_932836.2:n.3874G>A
|
|
|
XR_932837.3:n.3674G>A
|
|
|
XR_932838.3:n.3674G>A
|
|
|
NM_001171.6:c.3693G>A
MANE Select
|
NP_001162.5:p.Val1231=
|
|