NM_004525.3:c.13620+16G>A
MANE Select
|
NP_004516.2:n.13620+16G>A
|
ENST00000649046.1:c.13620+16G>A
MANE Select
|
ENSP00000496870.1:n.13620+16G>A
|
NM_004525.2:c.13620+16G>A
|
NP_004516.2:n.13620+16G>A
|
ENST00000263816.7:c.13620+16G>A
|
ENSP00000263816.3:n.13620+16G>A
|
ENST00000491228.1:n.474+16G>A
|
|
ENST00000649153.1:c.4429+16G>A
|
|
ENST00000650252.1:c.2611+16G>A
|
ENSP00000496887.1:n.2611+16G>A
|
XM_011511183.1:c.13491+16G>A
|
XP_011509485.1:n.13491+16G>A
|
XM_011511183.3:c.13491+16G>A
|
XP_011509485.1:n.13491+16G>A
|
XM_011511184.1:c.11331+16G>A
|
XP_011509486.1:n.11331+16G>A
|
XM_011511184.2:c.11331+16G>A
|
XP_011509486.1:n.11331+16G>A
|