ENST00000609686.4:c.1781-193C>A
MANE Select
|
ENSP00000477455.1:n.1781-193C>A
|
|
ENST00000628166.2:n.41-193C>A
|
|
|
ENST00000609686.3:c.1781-193C>A
|
ENSP00000477455.1:n.1781-193C>A
|
|
ENST00000628166.1:n.41-193C>A
|
|
|
NM_000834.3:c.1781-193C>A
|
NP_000825.2:n.1781-193C>A
|
|
XM_011520628.1:c.1781-193C>A
|
XP_011518930.1:n.1781-193C>A
|
|
XM_011520629.1:c.1781-193C>A
|
XP_011518931.1:n.1781-193C>A
|
|
XM_011520630.1:c.1781-193C>A
|
XP_011518932.1:n.1781-193C>A
|
|
XR_931372.1:n.179-6073G>T
|
|
|
XR_931373.1:n.318+268G>T
|
|
|
NM_000834.4:c.1781-193C>A
|
NP_000825.2:n.1781-193C>A
|
|
XM_011520628.2:c.1781-193C>A
|
XP_011518930.1:n.1781-193C>A
|
|
XM_011520629.2:c.1781-193C>A
|
XP_011518931.1:n.1781-193C>A
|
|
XM_017019219.2:c.1781-193C>A
|
XP_016874708.1:n.1781-193C>A
|
|
XR_001749013.1:n.457+268G>T
|
|
|
XR_931372.2:n.316-6073G>T
|
|
|
XR_931373.2:n.457+268G>T
|
|
|
NM_000834.5:c.1781-193C>A
MANE Select
|
NP_000825.2:n.1781-193C>A
|
|