ENST00000576204.6:n.753T>C
|
|
|
ENST00000622290.5:c.*62T>C
|
ENSP00000483331.2:n.*62T>C
|
|
ENST00000205557.12:c.3890T>C
MANE Select
|
ENSP00000205557.7:p.Ile1297Thr
|
|
ENST00000640696.1:c.704T>C
|
ENSP00000492197.1:p.Ile235Thr
|
|
ENST00000205557.11:c.3890T>C
|
ENSP00000205557.7:p.Ile1297Thr
|
|
ENST00000456970.6:c.3515T>C
|
ENSP00000405002.2:n.3515T>C
|
|
ENST00000576204.5:n.753T>C
|
|
|
ENST00000622290.4:c.*1099T>C
|
ENSP00000483331.1:n.*1099T>C
|
|
NM_001171.5:c.3890T>C
|
NP_001162.4:p.Ile1297Thr
|
|
XM_011522479.1:c.3857T>C
|
XP_011520781.1:p.Ile1286Thr
|
|
XM_011522480.1:c.3548T>C
|
XP_011520782.1:p.Ile1183Thr
|
|
XM_011522481.1:c.3548T>C
|
XP_011520783.1:p.Ile1183Thr
|
|
XR_932836.1:n.4188T>C
|
|
|
XR_932837.1:n.3926T>C
|
|
|
XR_932838.1:n.3989T>C
|
|
|
XR_933134.1:n.539-4757A>G
|
|
|
NM_001351800.1:c.3548T>C
|
NP_001338729.1:p.Ile1183Thr
|
|
NR_147784.1:n.3552T>C
|
|
|
XM_011522479.2:c.3857T>C
|
XP_011520781.1:p.Ile1286Thr
|
|
XM_011522481.3:c.3548T>C
|
XP_011520783.1:p.Ile1183Thr
|
|
XM_017023212.1:c.3722T>C
|
XP_016878701.1:p.Ile1241Thr
|
|
XM_024450261.1:c.3926T>C
|
XP_024306029.1:p.Ile1309Thr
|
|
XR_932836.2:n.4134T>C
|
|
|
XR_932837.3:n.3871T>C
|
|
|
XR_932838.3:n.3934T>C
|
|
|
NM_001171.6:c.3890T>C
MANE Select
|
NP_001162.5:p.Ile1297Thr
|
|