ENST00000371820.4:c.1662+11C>T
|
ENSP00000360885.4:n.1662+11C>T
|
|
ENST00000371817.8:c.1662+11C>T
MANE Select
|
ENSP00000360882.3:n.1662+11C>T
|
|
ENST00000371817.7:c.1662+11C>T
|
ENSP00000360882.3:n.1662+11C>T
|
|
ENST00000618395.4:c.1662+11C>T
|
ENSP00000481360.1:n.1662+11C>T
|
|
NM_000093.4:c.1662+11C>T
|
NP_000084.3:n.1662+11C>T
|
|
NM_001278074.1:c.1662+11C>T
|
NP_001265003.1:n.1662+11C>T
|
|
XR_929712.1:n.2064+11C>T
|
|
|
XR_929713.1:n.2064+11C>T
|
|
|
XM_017014266.2:c.1662+11C>T
|
XP_016869755.1:n.1662+11C>T
|
|
XR_001746183.1:n.2060+11C>T
|
|
|
NM_000093.5:c.1662+11C>T
MANE Select
|
NP_000084.3:n.1662+11C>T
|
|