ENST00000084798.9:c.286-1253G>C
(CA11)
MANE Select
|
ENSP00000084798.3:n.286-1253G>C
|
|
ENST00000084798.8:c.286-1253G>C
(CA11)
|
ENSP00000084798.3:n.286-1253G>C
|
|
ENST00000430145.3:n.48+3387C>G
(SEC1P)
|
|
|
ENST00000474419.5:n.76+3387C>G
(SEC1P)
|
|
|
ENST00000483163.1:n.76+3387C>G
(SEC1P)
|
|
|
NM_001217.3:c.286-1253G>C
(CA11)
|
NP_001208.2:n.286-1253G>C
|
|
NR_004401.2:n.108+3387C>G
(SEC1P)
|
|
|
NM_001217.4:c.286-1253G>C
(CA11)
|
NP_001208.2:n.286-1253G>C
|
|
NR_136241.1:n.966-1253G>C
(CA11)
|
|
|
XR_002958355.1:n.704-1253G>C
(CA11)
|
|
|
NM_001217.5:c.286-1253G>C
(CA11)
MANE Select
|
NP_001208.2:n.286-1253G>C
|
|
NR_136241.2:n.841-1253G>C
(CA11)
|
|
|