ENST00000272286.4:c.1971G>T
MANE Select
|
ENSP00000272286.2:p.Leu657=
|
|
ENST00000272286.2:c.1971G>T
|
ENSP00000272286.2:p.Leu657=
|
|
NM_022437.2:c.1971G>T
|
NP_071882.1:p.Leu657=
|
|
XM_005264483.2:c.1968G>T
|
XP_005264540.1:p.Leu656=
|
|
XM_011533029.1:c.1983G>T
|
XP_011531331.1:p.Leu661=
|
|
XM_011533030.1:c.1980G>T
|
XP_011531332.1:p.Leu660=
|
|
XM_011533031.1:c.1755G>T
|
XP_011531333.1:p.Leu585=
|
|
XR_939707.1:n.2473G>T
|
|
|
NM_001357321.1:c.1968G>T
|
NP_001344250.1:p.Leu656=
|
|
XM_011533029.2:c.1983G>T
|
XP_011531331.1:p.Leu661=
|
|
XM_011533030.2:c.1980G>T
|
XP_011531332.1:p.Leu660=
|
|
XR_001738891.1:n.2487G>T
|
|
|
XR_939707.2:n.2487G>T
|
|
|
NM_022437.3:c.1971G>T
MANE Select
|
NP_071882.1:p.Leu657=
|
|
NM_001357321.2:c.1968G>T
|
NP_001344250.1:p.Leu656=
|
|