ENST00000622290.5:c.3329G>T
|
ENSP00000483331.2:p.Cys1110Phe
|
|
ENST00000205557.12:c.3329G>T
MANE Select
|
ENSP00000205557.7:p.Cys1110Phe
|
|
ENST00000640696.1:c.321-1606G>T
|
ENSP00000492197.1:n.321-1606G>T
|
|
ENST00000205557.11:c.3329G>T
|
ENSP00000205557.7:p.Cys1110Phe
|
|
ENST00000456970.6:c.3132-1606G>T
|
ENSP00000405002.2:n.3132-1606G>T
|
|
ENST00000622290.4:c.*538G>T
|
ENSP00000483331.1:n.*538G>T
|
|
NM_001171.5:c.3329G>T
|
NP_001162.4:p.Cys1110Phe
|
|
XM_011522479.1:c.3296G>T
|
XP_011520781.1:p.Cys1099Phe
|
|
XM_011522480.1:c.2987G>T
|
XP_011520782.1:p.Cys996Phe
|
|
XM_011522481.1:c.2987G>T
|
XP_011520783.1:p.Cys996Phe
|
|
XR_932836.1:n.3564G>T
|
|
|
XR_932837.1:n.3543-1606G>T
|
|
|
XR_932838.1:n.3543-1606G>T
|
|
|
XR_933133.1:n.407+327C>A
|
|
|
XR_933134.1:n.754+327C>A
|
|
|
NM_001351800.1:c.2987G>T
|
NP_001338729.1:p.Cys996Phe
|
|
NR_147784.1:n.3169-1606G>T
|
|
|
XM_011522479.2:c.3296G>T
|
XP_011520781.1:p.Cys1099Phe
|
|
XM_011522481.3:c.2987G>T
|
XP_011520783.1:p.Cys996Phe
|
|
XM_017023212.1:c.3161G>T
|
XP_016878701.1:p.Cys1054Phe
|
|
XM_017023214.1:c.3307-1606G>T
|
XP_016878703.1:n.3307-1606G>T
|
|
XM_024450261.1:c.3365G>T
|
XP_024306029.1:p.Cys1122Phe
|
|
XR_932836.2:n.3510G>T
|
|
|
XR_932837.3:n.3488-1606G>T
|
|
|
XR_932838.3:n.3488-1606G>T
|
|
|
NM_001171.6:c.3329G>T
MANE Select
|
NP_001162.5:p.Cys1110Phe
|
|