ENST00000297784.10:c.1866T>A
MANE Select
|
ENSP00000297784.6:p.Pro622=
|
|
ENST00000644967.1:c.*306T>A
|
ENSP00000496159.1:n.*306T>A
|
|
ENST00000645053.1:c.1258-5925T>A
|
ENSP00000493838.1:n.1258-5925T>A
|
|
ENST00000645208.2:c.1866T>A
|
ENSP00000494684.1:p.Pro622=
|
|
ENST00000645773.1:c.1740T>A
|
ENSP00000493698.1:p.Pro580=
|
|
ENST00000645787.1:n.2009T>A
|
|
|
ENST00000646619.1:c.1428T>A
|
ENSP00000493726.1:p.Pro476=
|
|
ENST00000651183.1:c.1428T>A
|
ENSP00000498723.1:p.Pro476=
|
|
ENST00000297784.9:c.1866T>A
|
ENSP00000297784.5:p.Pro622=
|
|
ENST00000340019.4:c.1866T>A
|
ENSP00000341433.3:p.Pro622=
|
|
ENST00000469455.1:n.347T>A
|
|
|
ENST00000486417.5:n.764T>A
|
|
|
NM_138691.2:c.1866T>A
|
NP_619636.2:p.Pro622=
|
|
XM_011518213.1:c.2454T>A
|
XP_011516515.1:p.Pro818=
|
|
XM_017014256.1:c.1869T>A
|
XP_016869745.1:p.Pro623=
|
|
NM_138691.3:c.1866T>A
MANE Select
|
NP_619636.2:p.Pro622=
|
|