ENST00000297784.10:c.1939T>A
MANE Select
|
ENSP00000297784.6:p.Ser647Thr
|
|
ENST00000644967.1:c.*379T>A
|
ENSP00000496159.1:n.*379T>A
|
|
ENST00000645053.1:c.1258-5852T>A
|
ENSP00000493838.1:n.1258-5852T>A
|
|
ENST00000645208.2:c.1939T>A
|
ENSP00000494684.1:p.Ser647Thr
|
|
ENST00000645773.1:c.1813T>A
|
ENSP00000493698.1:p.Ser605Thr
|
|
ENST00000645787.1:n.2082T>A
|
|
|
ENST00000646619.1:c.1501T>A
|
ENSP00000493726.1:p.Ser501Thr
|
|
ENST00000651183.1:c.1501T>A
|
ENSP00000498723.1:p.Ser501Thr
|
|
ENST00000297784.9:c.1939T>A
|
ENSP00000297784.5:p.Ser647Thr
|
|
ENST00000340019.4:c.1939T>A
|
ENSP00000341433.3:p.Ser647Thr
|
|
ENST00000469455.1:n.420T>A
|
|
|
ENST00000486417.5:n.837T>A
|
|
|
NM_138691.2:c.1939T>A
|
NP_619636.2:p.Ser647Thr
|
|
XM_011518213.1:c.2527T>A
|
XP_011516515.1:p.Ser843Thr
|
|
XM_017014256.1:c.1942T>A
|
XP_016869745.1:p.Ser648Thr
|
|
NM_138691.3:c.1939T>A
MANE Select
|
NP_619636.2:p.Ser647Thr
|
|