ENST00000545968.6:c.2334_2335delinsCA
MANE Select
|
ENSP00000442795.1:p.Pro778=
|
|
ENST00000256993.8:c.2334_2335delinsCA
|
ENSP00000256993.5:p.Pro778=
|
|
ENST00000399249.6:c.2334_2335delinsCA
|
ENSP00000382193.2:p.Pro778=
|
|
ENST00000544791.1:c.2334_2335delinsCA
|
ENSP00000444259.1:p.Pro778=
|
|
ENST00000545968.5:c.2334_2335delinsCA
|
ENSP00000442795.1:p.Pro778=
|
|
NM_000256.3:c.2334_2335delinsCA , LRG_386t1:c.2334_2335delinsCA
MANE Select
|
NP_000247.2:p.Pro778=
|
|
XM_011520117.1:c.2316_2317delinsCA
|
XP_011518419.1:p.Pro772=
|
|
XM_011520118.1:c.2253_2254delinsCA
|
XP_011518420.1:p.Pro751=
|
|