ENST00000280097.5:c.624G>T
MANE Select
|
ENSP00000280097.3:p.Leu208=
|
|
ENST00000280097.4:c.624G>T
|
ENSP00000280097.3:p.Leu208=
|
|
ENST00000410115.5:c.624G>T
|
ENSP00000386940.1:p.Leu208=
|
|
ENST00000485653.1:n.556G>T
|
|
|
NM_006895.2:c.624G>T
|
NP_008826.1:p.Leu208=
|
|
XM_011511063.1:c.522G>T
|
XP_011509365.1:p.Leu174=
|
|
XM_011511064.1:c.246G>T
|
XP_011509366.1:p.Leu82=
|
|
XM_011511064.2:c.246G>T
|
XP_011509366.1:p.Leu82=
|
|
XM_017003948.1:c.522G>T
|
XP_016859437.1:p.Leu174=
|
|
XR_001739719.1:n.232-6079C>A
|
|
|
XR_002959286.1:n.1011G>T
|
|
|
NM_006895.3:c.624G>T
MANE Select
|
NP_008826.1:p.Leu208=
|
|