ENST00000697337.1:c.*2595+4A>T
|
ENSP00000513259.1:n.*2595+4A>T
|
|
ENST00000697338.1:c.1707+4A>T
|
ENSP00000513260.1:n.1707+4A>T
|
|
ENST00000697339.1:c.893+4A>T
|
ENSP00000513261.1:n.893+4A>T
|
|
ENST00000697340.1:c.*576+4A>T
|
ENSP00000513262.1:n.*576+4A>T
|
|
ENST00000697341.1:n.1829+4A>T
|
|
|
ENST00000313735.11:c.1859+4A>T
MANE Select
|
ENSP00000327251.6:n.1859+4A>T
|
|
ENST00000646938.1:c.1856+4A>T
|
ENSP00000494870.1:n.1856+4A>T
|
|
ENST00000313735.10:c.1859+4A>T
|
ENSP00000327251.6:n.1859+4A>T
|
|
ENST00000621962.1:c.1742+4A>T
|
ENSP00000482291.1:n.1742+4A>T
|
|
NM_000625.4:c.1859+4A>T
MANE Select
|
NP_000616.3:n.1859+4A>T
|
|
XM_011524859.1:c.1859+4A>T
|
XP_011523161.1:n.1859+4A>T
|
|
XM_011524860.1:c.1856+4A>T
|
XP_011523162.1:n.1856+4A>T
|
|
XM_011524861.1:c.1859+4A>T
|
XP_011523163.1:n.1859+4A>T
|
|
XM_011524862.1:c.1193+4A>T
|
XP_011523164.1:n.1193+4A>T
|
|