ENST00000697337.1:c.*3093-57G>C
|
ENSP00000513259.1:n.*3093-57G>C
|
|
ENST00000697338.1:c.2277-57G>C
|
ENSP00000513260.1:n.2277-57G>C
|
|
ENST00000697339.1:c.1391-57G>C
|
ENSP00000513261.1:n.1391-57G>C
|
|
ENST00000697340.1:c.*1146-61G>C
|
ENSP00000513262.1:n.*1146-61G>C
|
|
ENST00000697341.1:n.2399-57G>C
|
|
|
ENST00000313735.11:c.2429-57G>C
MANE Select
|
ENSP00000327251.6:n.2429-57G>C
|
|
ENST00000646938.1:c.2426-57G>C
|
ENSP00000494870.1:n.2426-57G>C
|
|
ENST00000313735.10:c.2429-57G>C
|
ENSP00000327251.6:n.2429-57G>C
|
|
ENST00000621962.1:c.2312-57G>C
|
ENSP00000482291.1:n.2312-57G>C
|
|
NM_000625.4:c.2429-57G>C
MANE Select
|
NP_000616.3:n.2429-57G>C
|
|
XM_011524859.1:c.2429-57G>C
|
XP_011523161.1:n.2429-57G>C
|
|
XM_011524860.1:c.2426-57G>C
|
XP_011523162.1:n.2426-57G>C
|
|
XM_011524861.1:c.2357-57G>C
|
XP_011523163.1:n.2357-57G>C
|
|
XM_011524862.1:c.1763-57G>C
|
XP_011523164.1:n.1763-57G>C
|
|