ENST00000311907.10:c.874+14G>C
MANE Select
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ENSP00000308541.5:n.874+14G>C
|
|
ENST00000311907.9:c.874+14G>C
|
ENSP00000308541.5:n.874+14G>C
|
|
ENST00000442468.1:c.844+14G>C
|
ENSP00000387413.1:n.844+14G>C
|
|
ENST00000530231.5:c.874+14G>C
|
ENSP00000433907.1:n.874+14G>C
|
|
NM_000506.3:c.874+14G>C
|
NP_000497.1:n.874+14G>C
|
|
NM_000506.4:c.874+14G>C , LRG_551t1:c.874+14G>C
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NP_000497.1:n.874+14G>C
|
|
NM_001311257.1:c.826+14G>C
|
NP_001298186.1:n.826+14G>C
|
|
XR_428840.2:n.918+14G>C
|
|
|
XR_428840.4:n.909+14G>C
|
|
|
NM_000506.5:c.874+14G>C
MANE Select
|
NP_000497.1:n.874+14G>C
|
|
NM_001311257.2:c.826+14G>C
|
NP_001298186.1:n.826+14G>C
|
|