ENST00000562955.2:c.8655-2A>G
|
ENSP00000457168.1:n.8655-2A>G
|
|
ENST00000634258.3:c.8826-2A>G
MANE Select
|
ENSP00000489255.1:n.8826-2A>G
|
|
ENST00000638263.1:n.180-2A>G
|
|
|
ENST00000640484.1:n.256A>G
|
|
|
ENST00000648058.1:n.5280-2A>G
|
|
|
ENST00000649403.1:n.3576-2A>G
|
|
|
ENST00000460536.1:n.641A>G
|
|
|
ENST00000562955.1:c.8655-2A>G
|
ENSP00000457168.1:n.8655-2A>G
|
|
ENST00000634258.1:c.8826-2A>G
|
ENSP00000489255.1:n.8826-2A>G
|
|
NM_015284.3:c.8655-2A>G
|
NP_056099.3:n.8655-2A>G
|
|
XM_005270686.2:c.8889-2A>G
|
XP_005270743.1:n.8889-2A>G
|
|
XM_006710501.2:c.8826-2A>G
|
XP_006710564.1:n.8826-2A>G
|
|
XM_011541103.1:c.8943-2A>G
|
XP_011539405.1:n.8943-2A>G
|
|
XM_011541104.1:c.8772-2A>G
|
XP_011539406.1:n.8772-2A>G
|
|
XM_011541105.1:c.8769-2A>G
|
XP_011539407.1:n.8769-2A>G
|
|
XM_011541106.1:c.8769-2A>G
|
XP_011539408.1:n.8769-2A>G
|
|
XM_011541107.1:c.8370-2A>G
|
XP_011539409.1:n.8370-2A>G
|
|
NM_001365999.1:c.8826-2A>G
MANE Select
|
NP_001352928.1:n.8826-2A>G
|
|
XM_005270686.3:c.8889-2A>G
|
XP_005270743.1:n.8889-2A>G
|
|
XM_011541106.3:c.8769-2A>G
|
XP_011539408.1:n.8769-2A>G
|
|
XM_011541107.2:c.8370-2A>G
|
XP_011539409.1:n.8370-2A>G
|
|
XM_017000819.1:c.8736-2A>G
|
XP_016856308.1:n.8736-2A>G
|
|
XM_017000820.1:c.8718-2A>G
|
XP_016856309.1:n.8718-2A>G
|
|
XM_017000821.1:c.7518-2A>G
|
XP_016856310.1:n.7518-2A>G
|
|
XR_001737075.1:n.8772-2A>G
|
|
|
XR_002956151.1:n.8772-2A>G
|
|
|
NM_015284.4:c.8655-2A>G
|
NP_056099.3:n.8655-2A>G
|
|