|
ENST00000396819.8:c.1161T>C
MANE Select
|
ENSP00000380031.5:p.Gly387=
|
|
|
ENST00000204005.13:c.1251T>C
|
ENSP00000204005.10:p.Gly417=
|
|
|
ENST00000308370.11:c.1362T>C
|
ENSP00000311905.8:p.Gly454=
|
|
|
ENST00000396819.7:c.1161T>C
|
ENSP00000380031.4:p.Gly387=
|
|
|
ENST00000595529.1:n.231T>C
|
|
|
|
ENST00000598717.5:n.429-3150T>C
|
|
|
|
NM_001042544.1:c.1362T>C
|
NP_001036009.1:p.Gly454=
|
|
|
NM_001042545.1:c.1161T>C
|
NP_001036010.1:p.Gly387=
|
|
|
NM_003573.2:c.1251T>C
|
NP_003564.2:p.Gly417=
|
|
|
XM_011527376.1:c.1362T>C
|
XP_011525678.1:p.Gly454=
|
|
|
XM_011527377.1:c.1395T>C
|
XP_011525679.1:p.Gly465=
|
|
|
XM_011527378.1:c.1395T>C
|
XP_011525680.1:p.Gly465=
|
|
|
XM_011527379.1:c.1161T>C
|
XP_011525681.1:p.Gly387=
|
|
|
XM_011527380.1:c.1395T>C
|
XP_011525682.1:p.Gly465=
|
|
|
XM_011527381.1:c.1395T>C
|
XP_011525683.1:p.Gly465=
|
|
|
XM_011527382.1:c.1395T>C
|
XP_011525684.1:p.Gly465=
|
|
|
XM_011527383.1:c.1395T>C
|
XP_011525685.1:p.Gly465=
|
|
|
XM_011527384.1:c.1395T>C
|
XP_011525686.1:p.Gly465=
|
|
|
XM_011527385.1:c.1395T>C
|
XP_011525687.1:p.Gly465=
|
|
|
XM_011527386.1:c.1395T>C
|
XP_011525688.1:p.Gly465=
|
|
|
XM_011527387.1:c.753T>C
|
XP_011525689.1:p.Gly251=
|
|
|
XM_011527376.2:c.1362T>C
|
XP_011525678.1:p.Gly454=
|
|
|
XM_011527377.2:c.1395T>C
|
XP_011525679.1:p.Gly465=
|
|
|
XM_011527378.2:c.1395T>C
|
XP_011525680.1:p.Gly465=
|
|
|
XM_011527380.2:c.1395T>C
|
XP_011525682.1:p.Gly465=
|
|
|
XM_011527381.2:c.1395T>C
|
XP_011525683.1:p.Gly465=
|
|
|
XM_011527382.2:c.1395T>C
|
XP_011525684.1:p.Gly465=
|
|
|
XM_011527383.2:c.1395T>C
|
XP_011525685.1:p.Gly465=
|
|
|
XM_011527384.2:c.1395T>C
|
XP_011525686.1:p.Gly465=
|
|
|
XM_011527385.2:c.1395T>C
|
XP_011525687.1:p.Gly465=
|
|
|
XM_011527386.2:c.1395T>C
|
XP_011525688.1:p.Gly465=
|
|
|
XM_017027352.1:c.1395T>C
|
XP_016882841.1:p.Gly465=
|
|
|
XM_017027353.1:c.1395T>C
|
XP_016882842.1:p.Gly465=
|
|
|
XM_017027354.1:c.1395T>C
|
XP_016882843.1:p.Gly465=
|
|
|
NM_001042545.2:c.1161T>C
MANE Select
|
NP_001036010.1:p.Gly387=
|
|
