ENST00000455537.7:c.2909+121A>C
MANE Select
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ENSP00000408979.2:n.2909+121A>C
|
|
ENST00000674619.1:c.2930+121A>C
|
ENSP00000502270.1:n.2930+121A>C
|
|
ENST00000675737.1:n.313+121A>C
|
|
|
ENST00000675882.1:n.2252A>C
|
|
|
ENST00000675929.1:n.1467+121A>C
|
|
|
ENST00000676457.1:c.2804+121A>C
|
ENSP00000501588.1:n.2804+121A>C
|
|
ENST00000286452.5:c.2642+121A>C
|
ENSP00000286452.5:n.2642+121A>C
|
|
ENST00000455537.6:c.2909+121A>C
|
ENSP00000408979.2:n.2909+121A>C
|
|
ENST00000552227.1:n.12A>C
|
|
|
NM_004984.2:c.2909+121A>C
|
NP_004975.2:n.2909+121A>C
|
|
NM_001354705.1:c.2642+121A>C
|
NP_001341634.1:n.2642+121A>C
|
|
NM_004984.3:c.2909+121A>C
|
NP_004975.2:n.2909+121A>C
|
|
XR_002957324.1:n.3142+121A>C
|
|
|
NM_004984.4:c.2909+121A>C
MANE Select
|
NP_004975.2:n.2909+121A>C
|
|
NM_001354705.2:c.2642+121A>C
|
NP_001341634.1:n.2642+121A>C
|
|