ENST00000373207.2:c.3067+17G>A
MANE Select
|
ENSP00000362303.1:n.3067+17G>A
|
|
ENST00000373207.1:c.3067+17G>A
|
ENSP00000362303.1:n.3067+17G>A
|
|
ENST00000373208.5:c.3076+17G>A
|
ENSP00000362304.1:n.3076+17G>A
|
|
NM_080722.3:c.3067+17G>A
|
NP_542453.2:n.3067+17G>A
|
|
NM_139155.2:c.3076+17G>A
|
NP_631894.2:n.3076+17G>A
|
|
XM_011539300.1:c.2566+17G>A
|
XP_011537602.1:n.2566+17G>A
|
|
XM_011539301.1:c.2140+17G>A
|
XP_011537603.1:n.2140+17G>A
|
|
XM_011539302.1:c.2140+17G>A
|
XP_011537604.1:n.2140+17G>A
|
|
XM_011539309.1:c.1636+17G>A
|
XP_011537611.1:n.1636+17G>A
|
|
NM_080722.4:c.3067+17G>A
MANE Select
|
NP_542453.2:n.3067+17G>A
|
|
NM_139155.3:c.3076+17G>A
|
NP_631894.2:n.3076+17G>A
|
|
XM_011539300.2:c.2566+17G>A
|
XP_011537602.1:n.2566+17G>A
|
|
XM_011539301.2:c.2140+17G>A
|
XP_011537603.1:n.2140+17G>A
|
|
XM_011539302.2:c.2140+17G>A
|
XP_011537604.1:n.2140+17G>A
|
|