ENST00000305249.10:c.390-34497A>C
MANE Select
|
ENSP00000303522.4:n.390-34497A>C
|
|
ENST00000305249.9:c.390-34497A>C
|
ENSP00000303522.4:n.390-34497A>C
|
|
ENST00000409848.3:c.390-34497A>C
|
ENSP00000386448.3:n.390-34497A>C
|
|
NM_001058.3:c.390-34497A>C
|
NP_001049.1:n.390-34497A>C
|
|
NM_015727.2:c.390-34497A>C
|
NP_056542.1:n.390-34497A>C
|
|
XR_940257.1:n.108+8805T>G
|
|
|
XR_940258.1:n.1323T>G
|
|
|
XR_940259.1:n.182+694T>G
|
|
|
XR_940257.2:n.109+8805T>G
|
|
|
NM_001058.4:c.390-34497A>C
MANE Select
|
NP_001049.1:n.390-34497A>C
|
|
NM_015727.3:c.390-34497A>C
|
NP_056542.1:n.390-34497A>C
|
|
NR_168009.1:n.254+694T>G
|
|
|
NR_168010.1:n.254+694T>G
|
|
|
NR_168011.1:n.254+694T>G
|
|
|