ENST00000297784.10:c.1767G>A
MANE Select
|
ENSP00000297784.6:p.Met589Ile
|
|
ENST00000644967.1:c.*207G>A
|
ENSP00000496159.1:n.*207G>A
|
|
ENST00000645053.1:c.1258-6024G>A
|
ENSP00000493838.1:n.1258-6024G>A
|
|
ENST00000645208.2:c.1767G>A
|
ENSP00000494684.1:p.Met589Ile
|
|
ENST00000645773.1:c.1641G>A
|
ENSP00000493698.1:p.Met547Ile
|
|
ENST00000645787.1:n.1910G>A
|
|
|
ENST00000646619.1:c.1329G>A
|
ENSP00000493726.1:p.Met443Ile
|
|
ENST00000651183.1:c.1329G>A
|
ENSP00000498723.1:p.Met443Ile
|
|
ENST00000297784.9:c.1767G>A
|
ENSP00000297784.5:p.Met589Ile
|
|
ENST00000340019.4:c.1767G>A
|
ENSP00000341433.3:p.Met589Ile
|
|
ENST00000469455.1:n.248G>A
|
|
|
ENST00000486417.5:n.665G>A
|
|
|
NM_138691.2:c.1767G>A
|
NP_619636.2:p.Met589Ile
|
|
XM_011518213.1:c.2355G>A
|
XP_011516515.1:p.Met785Ile
|
|
XM_017014256.1:c.1770G>A
|
XP_016869745.1:p.Met590Ile
|
|
NM_138691.3:c.1767G>A
MANE Select
|
NP_619636.2:p.Met589Ile
|
|