ENST00000280097.5:c.524G>T
MANE Select
|
ENSP00000280097.3:p.Gly175Val
|
|
ENST00000280097.4:c.524G>T
|
ENSP00000280097.3:p.Gly175Val
|
|
ENST00000410115.5:c.524G>T
|
ENSP00000386940.1:p.Gly175Val
|
|
ENST00000485653.1:n.456G>T
|
|
|
NM_006895.2:c.524G>T
|
NP_008826.1:p.Gly175Val
|
|
XM_011511063.1:c.422G>T
|
XP_011509365.1:p.Gly141Val
|
|
XM_011511064.1:c.146G>T
|
XP_011509366.1:p.Gly49Val
|
|
XM_011511064.2:c.146G>T
|
XP_011509366.1:p.Gly49Val
|
|
XM_017003948.1:c.422G>T
|
XP_016859437.1:p.Gly141Val
|
|
XR_001739719.1:n.232-5979C>A
|
|
|
XR_002959286.1:n.911G>T
|
|
|
NM_006895.3:c.524G>T
MANE Select
|
NP_008826.1:p.Gly175Val
|
|