|
NM_001725.3:c.1075G>A
MANE Select
|
NP_001716.3:p.Gly359Ser
|
|
ENST00000642449.2:c.1075G>A
MANE Select
|
ENSP00000494528.2:p.Gly359Ser
|
|
NM_001725.2:c.1087G>A
|
NP_001716.2:p.Gly363Ser
|
|
ENST00000262865.8:c.1087G>A
|
ENSP00000262865.4:p.Gly363Ser
|
|
ENST00000262865.9:c.1087G>A
|
ENSP00000262865.4:p.Gly363Ser
|
|
ENST00000417318.3:c.484G>A
|
ENSP00000409833.2:p.Gly162Ser
|
|
ENST00000489102.2:c.*264G>A
|
ENSP00000486976.1:n.*264G>A
|
|
XM_005260522.2:c.1087G>A
|
XP_005260579.1:p.Gly363Ser
|
|
XM_011529012.1:c.484G>A
|
XP_011527314.1:p.Gly162Ser
|
|
XM_024451972.1:c.493G>A
|
XP_024307740.1:p.Gly165Ser
|
|
XR_430313.2:n.1116G>A
|
|