ENST00000576204.6:n.904+11T>G
|
|
|
ENST00000622290.5:c.*213+11T>G
|
ENSP00000483331.2:n.*213+11T>G
|
|
ENST00000205557.12:c.4041+11T>G
MANE Select
|
ENSP00000205557.7:n.4041+11T>G
|
|
ENST00000640696.1:c.855+11T>G
|
ENSP00000492197.1:n.855+11T>G
|
|
ENST00000205557.11:c.4041+11T>G
|
ENSP00000205557.7:n.4041+11T>G
|
|
ENST00000456970.6:c.3666+11T>G
|
ENSP00000405002.2:n.3666+11T>G
|
|
ENST00000576204.5:n.904+11T>G
|
|
|
ENST00000622290.4:c.*1250+11T>G
|
ENSP00000483331.1:n.*1250+11T>G
|
|
NM_001171.5:c.4041+11T>G
|
NP_001162.4:n.4041+11T>G
|
|
XM_011522479.1:c.4008+11T>G
|
XP_011520781.1:n.4008+11T>G
|
|
XM_011522480.1:c.3699+11T>G
|
XP_011520782.1:n.3699+11T>G
|
|
XM_011522481.1:c.3699+11T>G
|
XP_011520783.1:n.3699+11T>G
|
|
XR_933134.1:n.539-4919A>C
|
|
|
NM_001351800.1:c.3699+11T>G
|
NP_001338729.1:n.3699+11T>G
|
|
NR_147784.1:n.3703+11T>G
|
|
|
XM_011522479.2:c.4008+11T>G
|
XP_011520781.1:n.4008+11T>G
|
|
XM_011522481.3:c.3699+11T>G
|
XP_011520783.1:n.3699+11T>G
|
|
XM_017023212.1:c.3873+11T>G
|
XP_016878701.1:n.3873+11T>G
|
|
XM_024450261.1:c.4077+11T>G
|
XP_024306029.1:n.4077+11T>G
|
|
NM_001171.6:c.4041+11T>G
MANE Select
|
NP_001162.5:n.4041+11T>G
|
|