ENST00000545968.6:c.1457+18G>C
MANE Select
|
ENSP00000442795.1:n.1457+18G>C
|
|
ENST00000256993.8:c.1457+18G>C
|
ENSP00000256993.5:n.1457+18G>C
|
|
ENST00000399249.6:c.1457+18G>C
|
ENSP00000382193.2:n.1457+18G>C
|
|
ENST00000544791.1:c.1457+18G>C
|
ENSP00000444259.1:n.1457+18G>C
|
|
ENST00000545968.5:c.1457+18G>C
|
ENSP00000442795.1:n.1457+18G>C
|
|
NM_000256.3:c.1457+18G>C , LRG_386t1:c.1457+18G>C
MANE Select
|
NP_000247.2:n.1457+18G>C
|
|
XM_011520117.1:c.1439+18G>C
|
XP_011518419.1:n.1439+18G>C
|
|
XM_011520118.1:c.1457+18G>C
|
XP_011518420.1:n.1457+18G>C
|
|