ENST00000297784.10:c.887T>C
MANE Select
|
ENSP00000297784.6:p.Met296Thr
|
|
ENST00000644967.1:c.449T>C
|
ENSP00000496159.1:p.Met150Thr
|
|
ENST00000645053.1:c.449T>C
|
ENSP00000493838.1:p.Met150Thr
|
|
ENST00000645208.2:c.887T>C
|
ENSP00000494684.1:p.Met296Thr
|
|
ENST00000645773.1:c.761T>C
|
ENSP00000493698.1:p.Met254Thr
|
|
ENST00000645787.1:n.927T>C
|
|
|
ENST00000646619.1:c.449T>C
|
ENSP00000493726.1:p.Met150Thr
|
|
ENST00000650689.1:n.1185T>C
|
|
|
ENST00000651183.1:c.449T>C
|
ENSP00000498723.1:p.Met150Thr
|
|
ENST00000297784.9:c.887T>C
|
ENSP00000297784.5:p.Met296Thr
|
|
ENST00000340019.4:c.887T>C
|
ENSP00000341433.3:p.Met296Thr
|
|
NM_138691.2:c.887T>C
|
NP_619636.2:p.Met296Thr
|
|
XM_011518213.1:c.1475T>C
|
XP_011516515.1:p.Met492Thr
|
|
XM_017014256.1:c.890T>C
|
XP_016869745.1:p.Met297Thr
|
|
NM_138691.3:c.887T>C
MANE Select
|
NP_619636.2:p.Met296Thr
|
|