ENST00000262367.10:c.2113+95T>C
MANE Select
|
ENSP00000262367.5:n.2113+95T>C
|
|
ENST00000262367.9:c.2113+95T>C
|
ENSP00000262367.5:n.2113+95T>C
|
|
ENST00000382070.7:c.1999+95T>C
|
ENSP00000371502.3:n.1999+95T>C
|
|
ENST00000570939.2:c.718+95T>C
|
ENSP00000461002.2:n.718+95T>C
|
|
ENST00000571826.5:c.162+95T>C
|
|
|
ENST00000572134.1:c.426+95T>C
|
|
|
NM_001079846.1:c.1999+95T>C
|
NP_001073315.1:n.1999+95T>C
|
|
NM_004380.2:c.2113+95T>C
|
NP_004371.2:n.2113+95T>C
|
|
XM_005255124.3:c.2113+95T>C
|
XP_005255181.1:n.2113+95T>C
|
|
XM_005255125.3:c.2113+95T>C
|
XP_005255182.1:n.2113+95T>C
|
|
XM_006720848.2:c.2113+95T>C
|
XP_006720911.1:n.2113+95T>C
|
|
XM_011522380.1:c.2059+95T>C
|
XP_011520682.1:n.2059+95T>C
|
|
XM_011522381.1:c.1360+95T>C
|
XP_011520683.1:n.1360+95T>C
|
|
XM_011522382.1:c.2113+95T>C
|
XP_011520684.1:n.2113+95T>C
|
|
XM_005255124.4:c.2113+95T>C
|
XP_005255181.1:n.2113+95T>C
|
|
XM_005255125.4:c.2113+95T>C
|
XP_005255182.1:n.2113+95T>C
|
|
XM_006720848.3:c.2113+95T>C
|
XP_006720911.1:n.2113+95T>C
|
|
XM_011522381.2:c.1360+95T>C
|
XP_011520683.1:n.1360+95T>C
|
|
XM_011522382.3:c.2113+95T>C
|
XP_011520684.1:n.2113+95T>C
|
|
XM_017022944.1:c.2113+95T>C
|
XP_016878433.1:n.2113+95T>C
|
|
NM_004380.3:c.2113+95T>C
MANE Select
|
NP_004371.2:n.2113+95T>C
|
|