ENST00000265080.9:c.288+26282T>C
MANE Select
|
ENSP00000265080.4:n.288+26282T>C
|
|
ENST00000638442.1:c.288+26282T>C
|
ENSP00000491428.1:n.288+26282T>C
|
|
ENST00000265080.8:c.288+26282T>C
|
ENSP00000265080.4:n.288+26282T>C
|
|
ENST00000503795.1:c.288+26282T>C
|
ENSP00000421771.1:n.288+26282T>C
|
|
NM_006909.2:c.288+26282T>C
|
NP_008840.1:n.288+26282T>C
|
|
XM_005248565.1:c.288+26282T>C
|
XP_005248622.1:n.288+26282T>C
|
|
XM_017009683.1:c.288+26282T>C
|
XP_016865172.1:n.288+26282T>C
|
|
XM_024446141.1:c.288+26282T>C
|
XP_024301909.1:n.288+26282T>C
|
|
XM_024446142.1:c.288+26282T>C
|
XP_024301910.1:n.288+26282T>C
|
|
XR_002956166.1:n.355+26282T>C
|
|
|
NM_006909.3:c.288+26282T>C
MANE Select
|
NP_008840.1:n.288+26282T>C
|
|