|
ENST00000265854.12:c.1416+268T>G
MANE Select
|
ENSP00000265854.7:n.1416+268T>G
|
|
|
ENST00000651235.1:c.*4176+268T>G
|
ENSP00000498895.1:n.*4176+268T>G
|
|
|
ENST00000265854.11:c.1416+268T>G
|
ENSP00000265854.7:n.1416+268T>G
|
|
|
ENST00000399654.6:c.1416+268T>G
|
ENSP00000382562.2:n.1416+268T>G
|
|
|
ENST00000402746.5:c.1140+268T>G
|
ENSP00000384155.1:n.1140+268T>G
|
|
|
ENST00000406869.5:c.1416+268T>G
|
ENSP00000385334.1:n.1416+268T>G
|
|
|
ENST00000438959.5:c.417+268T>G
|
ENSP00000414877.1:n.417+268T>G
|
|
|
ENST00000444373.6:c.186+268T>G
|
ENSP00000393037.2:n.186+268T>G
|
|
|
NM_001013836.1:c.1416+268T>G
|
NP_001013858.1:n.1416+268T>G
|
|
|
NM_001013837.1:c.1416+268T>G
|
NP_001013859.1:n.1416+268T>G
|
|
|
NM_001304523.1:c.1416+268T>G
|
NP_001291452.1:n.1416+268T>G
|
|
|
NM_001304524.1:c.1140+268T>G
|
NP_001291453.1:n.1140+268T>G
|
|
|
NM_003550.2:c.1416+268T>G
|
NP_003541.2:n.1416+268T>G
|
|
|
XM_005249877.1:c.1275+268T>G
|
XP_005249934.1:n.1275+268T>G
|
|
|
XM_011515567.1:c.1359+12705T>G
|
XP_011513869.1:n.1359+12705T>G
|
|
|
XM_011515568.1:c.1416+268T>G
|
XP_011513870.1:n.1416+268T>G
|
|
|
XM_011515569.1:c.186+268T>G
|
XP_011513871.1:n.186+268T>G
|
|
|
XM_011515571.1:c.186+268T>G
|
XP_011513873.1:n.186+268T>G
|
|
|
XM_011515568.3:c.1416+268T>G
|
XP_011513870.1:n.1416+268T>G
|
|
|
XM_011515569.3:c.450+268T>G
|
XP_011513871.2:n.450+268T>G
|
|
|
XM_017012690.1:c.1608+268T>G
|
XP_016868179.1:n.1608+268T>G
|
|
|
XM_017012691.2:c.186+268T>G
|
XP_016868180.1:n.186+268T>G
|
|
|
XM_024446951.1:c.1359+12705T>G
|
XP_024302719.1:n.1359+12705T>G
|
|
|
XM_024446952.1:c.1359+12705T>G
|
XP_024302720.1:n.1359+12705T>G
|
|
|
NM_001013836.2:c.1416+268T>G
MANE Select
|
NP_001013858.1:n.1416+268T>G
|
|
|
NM_001013837.2:c.1416+268T>G
|
NP_001013859.1:n.1416+268T>G
|
|
|
NM_001304523.2:c.1416+268T>G
|
NP_001291452.1:n.1416+268T>G
|
|
|
NM_001304524.2:c.1140+268T>G
|
NP_001291453.1:n.1140+268T>G
|
|
|
NM_003550.3:c.1416+268T>G
|
NP_003541.2:n.1416+268T>G
|
|
