ENST00000622290.5:c.3444T>G
|
ENSP00000483331.2:p.Ala1148=
|
|
ENST00000205557.12:c.3444T>G
MANE Select
|
ENSP00000205557.7:p.Ala1148=
|
|
ENST00000640696.1:c.321-1491T>G
|
ENSP00000492197.1:n.321-1491T>G
|
|
ENST00000205557.11:c.3444T>G
|
ENSP00000205557.7:p.Ala1148=
|
|
ENST00000456970.6:c.3132-1491T>G
|
ENSP00000405002.2:n.3132-1491T>G
|
|
ENST00000622290.4:c.*653T>G
|
ENSP00000483331.1:n.*653T>G
|
|
NM_001171.5:c.3444T>G
|
NP_001162.4:p.Ala1148=
|
|
XM_011522479.1:c.3411T>G
|
XP_011520781.1:p.Ala1137=
|
|
XM_011522480.1:c.3102T>G
|
XP_011520782.1:p.Ala1034=
|
|
XM_011522481.1:c.3102T>G
|
XP_011520783.1:p.Ala1034=
|
|
XR_932836.1:n.3679T>G
|
|
|
XR_932837.1:n.3543-1491T>G
|
|
|
XR_932838.1:n.3543-1491T>G
|
|
|
XR_933133.1:n.407+212A>C
|
|
|
XR_933134.1:n.754+212A>C
|
|
|
NM_001351800.1:c.3102T>G
|
NP_001338729.1:p.Ala1034=
|
|
NR_147784.1:n.3169-1491T>G
|
|
|
XM_011522479.2:c.3411T>G
|
XP_011520781.1:p.Ala1137=
|
|
XM_011522481.3:c.3102T>G
|
XP_011520783.1:p.Ala1034=
|
|
XM_017023212.1:c.3276T>G
|
XP_016878701.1:p.Ala1092=
|
|
XM_017023214.1:c.3307-1491T>G
|
XP_016878703.1:n.3307-1491T>G
|
|
XM_024450261.1:c.3480T>G
|
XP_024306029.1:p.Ala1160=
|
|
XR_932836.2:n.3625T>G
|
|
|
XR_932837.3:n.3488-1491T>G
|
|
|
XR_932838.3:n.3488-1491T>G
|
|
|
NM_001171.6:c.3444T>G
MANE Select
|
NP_001162.5:p.Ala1148=
|
|