ENST00000409709.9:c.6642C>A
MANE Select
|
ENSP00000386331.3:p.Gly2214=
|
|
ENST00000670577.1:c.4443C>A
|
|
|
ENST00000409619.6:c.6495C>A
|
ENSP00000386635.2:p.Gly2165=
|
|
ENST00000409709.7:c.6642C>A
|
ENSP00000386331.3:p.Gly2214=
|
|
ENST00000458169.2:c.4068C>A
|
ENSP00000417017.2:p.Gly1356=
|
|
ENST00000458637.6:c.6522C>A
|
ENSP00000392185.2:p.Gly2174=
|
|
ENST00000481328.7:n.5192C>A
|
|
|
ENST00000605744.1:n.2156C>A
|
|
|
NM_000260.3:c.6642C>A
|
NP_000251.3:p.Gly2214=
|
|
NM_001127180.1:c.6522C>A
|
NP_001120652.1:p.Gly2174=
|
|
XM_005274012.2:c.6525C>A
|
XP_005274069.1:p.Gly2175=
|
|
XM_006718561.2:c.6528C>A
|
XP_006718624.1:p.Gly2176=
|
|
XR_949941.1:n.6936C>A
|
|
|
XM_017017780.1:c.6732C>A
|
XP_016873269.1:p.Gly2244=
|
|
XM_017017784.1:c.6615C>A
|
XP_016873273.1:p.Gly2205=
|
|
XM_017017788.1:c.6618C>A
|
XP_016873277.1:p.Gly2206=
|
|
XR_001747885.1:n.6721C>A
|
|
|
XR_001747887.1:n.6707C>A
|
|
|
NM_000260.4:c.6642C>A
MANE Select
|
NP_000251.3:p.Gly2214=
|
|
NM_001127180.2:c.6522C>A
|
NP_001120652.1:p.Gly2174=
|
|
NM_001369365.1:c.6495C>A
|
NP_001356294.1:p.Gly2165=
|
|