ENST00000622290.5:c.3711G>C
|
ENSP00000483331.2:p.Gln1237His
|
|
ENST00000205557.12:c.3711G>C
MANE Select
|
ENSP00000205557.7:p.Gln1237His
|
|
ENST00000640696.1:c.525G>C
|
ENSP00000492197.1:p.Gln175His
|
|
ENST00000205557.11:c.3711G>C
|
ENSP00000205557.7:p.Gln1237His
|
|
ENST00000456970.6:c.3336G>C
|
ENSP00000405002.2:n.3336G>C
|
|
ENST00000622290.4:c.*920G>C
|
ENSP00000483331.1:n.*920G>C
|
|
NM_001171.5:c.3711G>C
|
NP_001162.4:p.Gln1237His
|
|
XM_011522479.1:c.3678G>C
|
XP_011520781.1:p.Gln1226His
|
|
XM_011522480.1:c.3369G>C
|
XP_011520782.1:p.Gln1123His
|
|
XM_011522481.1:c.3369G>C
|
XP_011520783.1:p.Gln1123His
|
|
XR_932836.1:n.3946G>C
|
|
|
XR_932837.1:n.3747G>C
|
|
|
XR_932838.1:n.3747G>C
|
|
|
XR_933134.1:n.539-275C>G
|
|
|
NM_001351800.1:c.3369G>C
|
NP_001338729.1:p.Gln1123His
|
|
NR_147784.1:n.3373G>C
|
|
|
XM_011522479.2:c.3678G>C
|
XP_011520781.1:p.Gln1226His
|
|
XM_011522481.3:c.3369G>C
|
XP_011520783.1:p.Gln1123His
|
|
XM_017023212.1:c.3543G>C
|
XP_016878701.1:p.Gln1181His
|
|
XM_024450261.1:c.3747G>C
|
XP_024306029.1:p.Gln1249His
|
|
XR_932836.2:n.3892G>C
|
|
|
XR_932837.3:n.3692G>C
|
|
|
XR_932838.3:n.3692G>C
|
|
|
NM_001171.6:c.3711G>C
MANE Select
|
NP_001162.5:p.Gln1237His
|
|