ENST00000272286.4:c.1829G>C
MANE Select
|
ENSP00000272286.2:p.Arg610Thr
|
|
ENST00000272286.2:c.1829G>C
|
ENSP00000272286.2:p.Arg610Thr
|
|
NM_022437.2:c.1829G>C
|
NP_071882.1:p.Arg610Thr
|
|
XM_005264483.2:c.1826G>C
|
XP_005264540.1:p.Arg609Thr
|
|
XM_011533029.1:c.1841G>C
|
XP_011531331.1:p.Arg614Thr
|
|
XM_011533030.1:c.1838G>C
|
XP_011531332.1:p.Arg613Thr
|
|
XM_011533031.1:c.1613G>C
|
XP_011531333.1:p.Arg538Thr
|
|
XR_939707.1:n.2331G>C
|
|
|
NM_001357321.1:c.1826G>C
|
NP_001344250.1:p.Arg609Thr
|
|
XM_011533029.2:c.1841G>C
|
XP_011531331.1:p.Arg614Thr
|
|
XM_011533030.2:c.1838G>C
|
XP_011531332.1:p.Arg613Thr
|
|
XR_001738891.1:n.2345G>C
|
|
|
XR_939707.2:n.2345G>C
|
|
|
NM_022437.3:c.1829G>C
MANE Select
|
NP_071882.1:p.Arg610Thr
|
|
NM_001357321.2:c.1826G>C
|
NP_001344250.1:p.Arg609Thr
|
|