ENST00000262367.10:c.3983-2A>G
MANE Select
|
ENSP00000262367.5:n.3983-2A>G
|
|
ENST00000262367.9:c.3983-2A>G
|
ENSP00000262367.5:n.3983-2A>G
|
|
ENST00000382070.7:c.3869-2A>G
|
ENSP00000371502.3:n.3869-2A>G
|
|
ENST00000570939.2:c.2618-2A>G
|
ENSP00000461002.2:n.2618-2A>G
|
|
ENST00000572569.1:n.447-2A>G
|
|
|
ENST00000573517.6:c.289-2A>G
|
|
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ENST00000574740.1:n.65-2A>G
|
|
|
ENST00000576720.1:n.2918A>G
|
|
|
NM_001079846.1:c.3869-2A>G
|
NP_001073315.1:n.3869-2A>G
|
|
NM_004380.2:c.3983-2A>G
|
NP_004371.2:n.3983-2A>G
|
|
XM_005255124.3:c.3938-2A>G
|
XP_005255181.1:n.3938-2A>G
|
|
XM_005255125.3:c.3566-2A>G
|
XP_005255182.1:n.3566-2A>G
|
|
XM_006720848.2:c.3983-2A>G
|
XP_006720911.1:n.3983-2A>G
|
|
XM_011522380.1:c.3929-2A>G
|
XP_011520682.1:n.3929-2A>G
|
|
XM_011522381.1:c.3230-2A>G
|
XP_011520683.1:n.3230-2A>G
|
|
XM_005255124.4:c.3938-2A>G
|
XP_005255181.1:n.3938-2A>G
|
|
XM_005255125.4:c.3566-2A>G
|
XP_005255182.1:n.3566-2A>G
|
|
XM_006720848.3:c.3983-2A>G
|
XP_006720911.1:n.3983-2A>G
|
|
XM_011522381.2:c.3230-2A>G
|
XP_011520683.1:n.3230-2A>G
|
|
XM_017022944.1:c.3977-2A>G
|
XP_016878433.1:n.3977-2A>G
|
|
NM_004380.3:c.3983-2A>G
MANE Select
|
NP_004371.2:n.3983-2A>G
|
|