ENST00000220616.9:c.8102G>C
MANE Select
|
ENSP00000220616.4:p.Ser2701Thr
|
|
ENST00000220616.8:c.8102G>C
|
ENSP00000220616.4:p.Ser2701Thr
|
|
ENST00000519178.5:c.3468G>C
|
|
|
ENST00000519543.5:c.2501G>C
|
ENSP00000430430.1:p.Ser834Thr
|
|
ENST00000521107.1:c.314G>C
|
ENSP00000430161.1:p.Ser105Thr
|
|
ENST00000522691.1:n.188G>C
|
|
|
ENST00000523756.5:c.4757G>C
|
|
|
NM_003235.4:c.8102G>C
|
NP_003226.4:p.Ser2701Thr
|
|
XM_005251038.3:c.7910G>C
|
XP_005251095.1:p.Ser2637Thr
|
|
XM_006716622.2:c.8039G>C
|
XP_006716685.1:p.Ser2680Thr
|
|
XM_005251038.4:c.7910G>C
|
XP_005251095.1:p.Ser2637Thr
|
|
XM_006716622.3:c.8039G>C
|
XP_006716685.1:p.Ser2680Thr
|
|
XM_017013793.1:c.8036G>C
|
XP_016869282.1:p.Ser2679Thr
|
|
XM_017013794.1:c.7967G>C
|
XP_016869283.1:p.Ser2656Thr
|
|
XM_017013795.1:c.7931G>C
|
XP_016869284.1:p.Ser2644Thr
|
|
XM_017013796.1:c.7883G>C
|
XP_016869285.1:p.Ser2628Thr
|
|
XM_017013797.1:c.7841G>C
|
XP_016869286.1:p.Ser2614Thr
|
|
NM_003235.5:c.8102G>C
MANE Select
|
NP_003226.4:p.Ser2701Thr
|
|