ENST00000297784.10:c.1885G>T
MANE Select
|
ENSP00000297784.6:p.Ala629Ser
|
|
ENST00000644967.1:c.*325G>T
|
ENSP00000496159.1:n.*325G>T
|
|
ENST00000645053.1:c.1258-5906G>T
|
ENSP00000493838.1:n.1258-5906G>T
|
|
ENST00000645208.2:c.1885G>T
|
ENSP00000494684.1:p.Ala629Ser
|
|
ENST00000645773.1:c.1759G>T
|
ENSP00000493698.1:p.Ala587Ser
|
|
ENST00000645787.1:n.2028G>T
|
|
|
ENST00000646619.1:c.1447G>T
|
ENSP00000493726.1:p.Ala483Ser
|
|
ENST00000651183.1:c.1447G>T
|
ENSP00000498723.1:p.Ala483Ser
|
|
ENST00000297784.9:c.1885G>T
|
ENSP00000297784.5:p.Ala629Ser
|
|
ENST00000340019.4:c.1885G>T
|
ENSP00000341433.3:p.Ala629Ser
|
|
ENST00000469455.1:n.366G>T
|
|
|
ENST00000486417.5:n.783G>T
|
|
|
NM_138691.2:c.1885G>T
|
NP_619636.2:p.Ala629Ser
|
|
XM_011518213.1:c.2473G>T
|
XP_011516515.1:p.Ala825Ser
|
|
XM_017014256.1:c.1888G>T
|
XP_016869745.1:p.Ala630Ser
|
|
NM_138691.3:c.1885G>T
MANE Select
|
NP_619636.2:p.Ala629Ser
|
|