ENST00000284292.11:c.15+2166G>C
MANE Select
|
ENSP00000284292.5:n.15+2166G>C
|
|
ENST00000284292.10:c.15+2166G>C
|
ENSP00000284292.5:n.15+2166G>C
|
|
ENST00000412681.2:c.15+2166G>C
|
ENSP00000399591.1:n.15+2166G>C
|
|
NM_001126181.1:c.15+2166G>C
|
NP_001119653.1:n.15+2166G>C
|
|
NM_006176.2:c.15+2166G>C
|
NP_006167.1:n.15+2166G>C
|
|
XR_429013.2:n.2318C>G
|
|
|
XR_948129.1:n.1806C>G
|
|
|
XR_948130.1:n.1339C>G
|
|
|
XR_948131.1:n.2135C>G
|
|
|
NM_006176.3:c.15+2166G>C
MANE Select
|
NP_006167.1:n.15+2166G>C
|
|
NM_001126181.2:c.15+2166G>C
|
NP_001119653.1:n.15+2166G>C
|
|