ENST00000220616.9:c.8165T>C
MANE Select
|
ENSP00000220616.4:p.Ile2722Thr
|
|
ENST00000220616.8:c.8165T>C
|
ENSP00000220616.4:p.Ile2722Thr
|
|
ENST00000519178.5:c.3531T>C
|
|
|
ENST00000519543.5:c.2564T>C
|
ENSP00000430430.1:p.Ile855Thr
|
|
ENST00000521107.1:c.377T>C
|
ENSP00000430161.1:p.Ile126Thr
|
|
ENST00000522691.1:n.251T>C
|
|
|
ENST00000523756.5:c.4820T>C
|
|
|
NM_003235.4:c.8165T>C
|
NP_003226.4:p.Ile2722Thr
|
|
XM_005251038.3:c.7973T>C
|
XP_005251095.1:p.Ile2658Thr
|
|
XM_006716622.2:c.8102T>C
|
XP_006716685.1:p.Ile2701Thr
|
|
XM_005251038.4:c.7973T>C
|
XP_005251095.1:p.Ile2658Thr
|
|
XM_006716622.3:c.8102T>C
|
XP_006716685.1:p.Ile2701Thr
|
|
XM_017013793.1:c.8099T>C
|
XP_016869282.1:p.Ile2700Thr
|
|
XM_017013794.1:c.8030T>C
|
XP_016869283.1:p.Ile2677Thr
|
|
XM_017013795.1:c.7994T>C
|
XP_016869284.1:p.Ile2665Thr
|
|
XM_017013796.1:c.7946T>C
|
XP_016869285.1:p.Ile2649Thr
|
|
XM_017013797.1:c.7904T>C
|
XP_016869286.1:p.Ile2635Thr
|
|
NM_003235.5:c.8165T>C
MANE Select
|
NP_003226.4:p.Ile2722Thr
|
|