ENST00000272286.4:c.1988G>C
MANE Select
|
ENSP00000272286.2:p.Arg663Thr
|
|
ENST00000272286.2:c.1988G>C
|
ENSP00000272286.2:p.Arg663Thr
|
|
NM_022437.2:c.1988G>C
|
NP_071882.1:p.Arg663Thr
|
|
XM_005264483.2:c.1985G>C
|
XP_005264540.1:p.Arg662Thr
|
|
XM_011533029.1:c.2000G>C
|
XP_011531331.1:p.Arg667Thr
|
|
XM_011533030.1:c.1997G>C
|
XP_011531332.1:p.Arg666Thr
|
|
XM_011533031.1:c.1772G>C
|
XP_011531333.1:p.Arg591Thr
|
|
XR_939707.1:n.2490G>C
|
|
|
NM_001357321.1:c.1985G>C
|
NP_001344250.1:p.Arg662Thr
|
|
XM_011533029.2:c.2000G>C
|
XP_011531331.1:p.Arg667Thr
|
|
XM_011533030.2:c.1997G>C
|
XP_011531332.1:p.Arg666Thr
|
|
XR_001738891.1:n.2504G>C
|
|
|
XR_939707.2:n.2504G>C
|
|
|
NM_022437.3:c.1988G>C
MANE Select
|
NP_071882.1:p.Arg663Thr
|
|
NM_001357321.2:c.1985G>C
|
NP_001344250.1:p.Arg662Thr
|
|