ENST00000622290.5:c.3479T>G
|
ENSP00000483331.2:p.Ile1160Ser
|
|
ENST00000205557.12:c.3479T>G
MANE Select
|
ENSP00000205557.7:p.Ile1160Ser
|
|
ENST00000640696.1:c.321-1456T>G
|
ENSP00000492197.1:n.321-1456T>G
|
|
ENST00000205557.11:c.3479T>G
|
ENSP00000205557.7:p.Ile1160Ser
|
|
ENST00000456970.6:c.3132-1456T>G
|
ENSP00000405002.2:n.3132-1456T>G
|
|
ENST00000622290.4:c.*688T>G
|
ENSP00000483331.1:n.*688T>G
|
|
NM_001171.5:c.3479T>G
|
NP_001162.4:p.Ile1160Ser
|
|
XM_011522479.1:c.3446T>G
|
XP_011520781.1:p.Ile1149Ser
|
|
XM_011522480.1:c.3137T>G
|
XP_011520782.1:p.Ile1046Ser
|
|
XM_011522481.1:c.3137T>G
|
XP_011520783.1:p.Ile1046Ser
|
|
XR_932836.1:n.3714T>G
|
|
|
XR_932837.1:n.3543-1456T>G
|
|
|
XR_932838.1:n.3543-1456T>G
|
|
|
XR_933133.1:n.407+177A>C
|
|
|
XR_933134.1:n.754+177A>C
|
|
|
NM_001351800.1:c.3137T>G
|
NP_001338729.1:p.Ile1046Ser
|
|
NR_147784.1:n.3169-1456T>G
|
|
|
XM_011522479.2:c.3446T>G
|
XP_011520781.1:p.Ile1149Ser
|
|
XM_011522481.3:c.3137T>G
|
XP_011520783.1:p.Ile1046Ser
|
|
XM_017023212.1:c.3311T>G
|
XP_016878701.1:p.Ile1104Ser
|
|
XM_017023214.1:c.3307-1456T>G
|
XP_016878703.1:n.3307-1456T>G
|
|
XM_024450261.1:c.3515T>G
|
XP_024306029.1:p.Ile1172Ser
|
|
XR_932836.2:n.3660T>G
|
|
|
XR_932837.3:n.3488-1456T>G
|
|
|
XR_932838.3:n.3488-1456T>G
|
|
|
NM_001171.6:c.3479T>G
MANE Select
|
NP_001162.5:p.Ile1160Ser
|
|