ENST00000272286.4:c.1854G>C
MANE Select
|
ENSP00000272286.2:p.Gly618=
|
|
ENST00000272286.2:c.1854G>C
|
ENSP00000272286.2:p.Gly618=
|
|
NM_022437.2:c.1854G>C
|
NP_071882.1:p.Gly618=
|
|
XM_005264483.2:c.1851G>C
|
XP_005264540.1:p.Gly617=
|
|
XM_011533029.1:c.1866G>C
|
XP_011531331.1:p.Gly622=
|
|
XM_011533030.1:c.1863G>C
|
XP_011531332.1:p.Gly621=
|
|
XM_011533031.1:c.1638G>C
|
XP_011531333.1:p.Gly546=
|
|
XR_939707.1:n.2356G>C
|
|
|
NM_001357321.1:c.1851G>C
|
NP_001344250.1:p.Gly617=
|
|
XM_011533029.2:c.1866G>C
|
XP_011531331.1:p.Gly622=
|
|
XM_011533030.2:c.1863G>C
|
XP_011531332.1:p.Gly621=
|
|
XR_001738891.1:n.2370G>C
|
|
|
XR_939707.2:n.2370G>C
|
|
|
NM_022437.3:c.1854G>C
MANE Select
|
NP_071882.1:p.Gly618=
|
|
NM_001357321.2:c.1851G>C
|
NP_001344250.1:p.Gly617=
|
|