ENST00000297784.10:c.1864C>G
MANE Select
|
ENSP00000297784.6:p.Pro622Ala
|
|
ENST00000644967.1:c.*304C>G
|
ENSP00000496159.1:n.*304C>G
|
|
ENST00000645053.1:c.1258-5927C>G
|
ENSP00000493838.1:n.1258-5927C>G
|
|
ENST00000645208.2:c.1864C>G
|
ENSP00000494684.1:p.Pro622Ala
|
|
ENST00000645773.1:c.1738C>G
|
ENSP00000493698.1:p.Pro580Ala
|
|
ENST00000645787.1:n.2007C>G
|
|
|
ENST00000646619.1:c.1426C>G
|
ENSP00000493726.1:p.Pro476Ala
|
|
ENST00000651183.1:c.1426C>G
|
ENSP00000498723.1:p.Pro476Ala
|
|
ENST00000297784.9:c.1864C>G
|
ENSP00000297784.5:p.Pro622Ala
|
|
ENST00000340019.4:c.1864C>G
|
ENSP00000341433.3:p.Pro622Ala
|
|
ENST00000469455.1:n.345C>G
|
|
|
ENST00000486417.5:n.762C>G
|
|
|
NM_138691.2:c.1864C>G
|
NP_619636.2:p.Pro622Ala
|
|
XM_011518213.1:c.2452C>G
|
XP_011516515.1:p.Pro818Ala
|
|
XM_017014256.1:c.1867C>G
|
XP_016869745.1:p.Pro623Ala
|
|
NM_138691.3:c.1864C>G
MANE Select
|
NP_619636.2:p.Pro622Ala
|
|