|
ENST00000692049.1:c.1755T>C
(ELN)
|
ENSP00000510104.1:p.Gly585=
|
|
|
ENST00000252034.12:c.1668T>C
(ELN)
MANE Select
|
ENSP00000252034.7:p.Gly556=
|
|
|
ENST00000252034.11:c.1668T>C
(ELN)
|
ENSP00000252034.7:p.Gly556=
|
|
|
ENST00000320399.10:c.1668T>C
(ELN)
|
ENSP00000313565.6:p.Gly556=
|
|
|
ENST00000320492.11:c.1425T>C
(ELN)
|
ENSP00000315607.7:p.Gly475=
|
|
|
ENST00000357036.9:c.1683T>C
(ELN)
|
ENSP00000349540.5:p.Gly561=
|
|
|
ENST00000358929.8:c.1755T>C
(ELN)
|
ENSP00000351807.5:p.Gly585=
|
|
|
ENST00000380553.8:c.1260T>C
(ELN)
|
ENSP00000369926.4:p.Gly420=
|
|
|
ENST00000380562.8:c.1686T>C
(ELN)
|
ENSP00000369936.4:p.Gly562=
|
|
|
ENST00000380575.8:c.1581T>C
(ELN)
|
ENSP00000369949.4:p.Gly527=
|
|
|
ENST00000380576.9:c.1611T>C
(ELN)
|
ENSP00000369950.5:p.Gly537=
|
|
|
ENST00000380584.8:c.1524T>C
(ELN)
|
ENSP00000369958.4:p.Gly508=
|
|
|
ENST00000414324.5:c.1596T>C
(ELN)
|
ENSP00000392575.1:p.Gly532=
|
|
|
ENST00000429192.5:c.1626T>C
(ELN)
|
ENSP00000391129.1:p.Gly542=
|
|
|
ENST00000445912.5:c.1668T>C
(ELN)
|
ENSP00000389857.1:p.Gly556=
|
|
|
ENST00000458204.5:c.1638T>C
(ELN)
|
ENSP00000403162.1:p.Gly546=
|
|
|
ENST00000621115.4:c.1401T>C
(ELN)
|
ENSP00000480955.1:p.Gly467=
|
|
|
NM_000501.3:c.1668T>C
(ELN)
|
NP_000492.2:p.Gly556=
|
|
|
NM_001081752.2:c.1581T>C
(ELN)
|
NP_001075221.1:p.Gly527=
|
|
|
NM_001081753.2:c.1626T>C
(ELN)
|
NP_001075222.1:p.Gly542=
|
|
|
NM_001081754.2:c.1683T>C
(ELN)
|
NP_001075223.1:p.Gly561=
|
|
|
NM_001081755.2:c.1611T>C
(ELN)
|
NP_001075224.1:p.Gly537=
|
|
|
NM_001278912.1:c.1668T>C
(ELN)
|
NP_001265841.1:p.Gly556=
|
|
|
NM_001278913.1:c.1425T>C
(ELN)
|
NP_001265842.1:p.Gly475=
|
|
|
NM_001278914.1:c.1596T>C
(ELN)
|
NP_001265843.1:p.Gly532=
|
|
|
NM_001278915.1:c.1686T>C
(ELN)
|
NP_001265844.1:p.Gly562=
|
|
|
NM_001278916.1:c.1524T>C
(ELN)
|
NP_001265845.1:p.Gly508=
|
|
|
NM_001278917.1:c.1638T>C
(ELN)
|
NP_001265846.1:p.Gly546=
|
|
|
NM_001278918.1:c.1401T>C
(ELN)
|
NP_001265847.1:p.Gly467=
|
|
|
NM_001278939.1:c.1755T>C
(ELN)
|
NP_001265868.1:p.Gly585=
|
|
|
XM_005250187.1:c.1632T>C
(ELN)
|
XP_005250244.1:p.Gly544=
|
|
|
XM_005250188.1:c.1626T>C
(ELN)
|
XP_005250245.1:p.Gly542=
|
|
|
XM_011515868.1:c.1683T>C
(ELN)
|
XP_011514170.1:p.Gly561=
|
|
|
XM_011515869.1:c.1653T>C
(ELN)
|
XP_011514171.1:p.Gly551=
|
|
|
XM_011515870.1:c.1647T>C
(ELN)
|
XP_011514172.1:p.Gly549=
|
|
|
XM_011515871.1:c.1641T>C
(ELN)
|
XP_011514173.1:p.Gly547=
|
|
|
XM_011515872.1:c.1629T>C
(ELN)
|
XP_011514174.1:p.Gly543=
|
|
|
XM_011515873.1:c.1626T>C
(ELN)
|
XP_011514175.1:p.Gly542=
|
|
|
XM_011515874.1:c.1617T>C
(ELN)
|
XP_011514176.1:p.Gly539=
|
|
|
XM_011515875.1:c.1602T>C
(ELN)
|
XP_011514177.1:p.Gly534=
|
|
|
XM_011515876.1:c.1683T>C
(ELN)
|
XP_011514178.1:p.Gly561=
|
|
|
XM_011515877.1:c.1572T>C
(ELN)
|
XP_011514179.1:p.Gly524=
|
|
|
XM_005250187.2:c.1632T>C
(ELN)
|
XP_005250244.1:p.Gly544=
|
|
|
XM_005250188.2:c.1626T>C
(ELN)
|
XP_005250245.1:p.Gly542=
|
|
|
XM_011515868.2:c.1683T>C
(ELN)
|
XP_011514170.1:p.Gly561=
|
|
|
XM_011515871.2:c.1641T>C
(ELN)
|
XP_011514173.1:p.Gly547=
|
|
|
XM_011515872.2:c.1629T>C
(ELN)
|
XP_011514174.1:p.Gly543=
|
|
|
XM_011515873.2:c.1626T>C
(ELN)
|
XP_011514175.1:p.Gly542=
|
|
|
XM_011515875.2:c.1602T>C
(ELN)
|
XP_011514177.1:p.Gly534=
|
|
|
XM_011515876.2:c.1683T>C
(ELN)
|
XP_011514178.1:p.Gly561=
|
|
|
XM_011515877.2:c.1572T>C
(ELN)
|
XP_011514179.1:p.Gly524=
|
|
|
XM_017011813.1:c.1596T>C
(ELN)
|
XP_016867302.1:p.Gly532=
|
|
|
XM_017011814.2:c.1584T>C
(ELN)
|
XP_016867303.1:p.Gly528=
|
|
|
XR_001745243.1:n.76-390A>G
(ELN-AS1)
|
|
|
|
NM_000501.4:c.1668T>C
(ELN)
MANE Select
|
NP_000492.2:p.Gly556=
|
|
|
NM_001081752.3:c.1581T>C
(ELN)
|
NP_001075221.1:p.Gly527=
|
|
|
NM_001081753.3:c.1626T>C
(ELN)
|
NP_001075222.1:p.Gly542=
|
|
|
NM_001081754.3:c.1683T>C
(ELN)
|
NP_001075223.1:p.Gly561=
|
|
|
NM_001081755.3:c.1611T>C
(ELN)
|
NP_001075224.1:p.Gly537=
|
|
|
NM_001278912.2:c.1668T>C
(ELN)
|
NP_001265841.1:p.Gly556=
|
|
|
NM_001278913.2:c.1425T>C
(ELN)
|
NP_001265842.1:p.Gly475=
|
|
|
NM_001278914.2:c.1596T>C
(ELN)
|
NP_001265843.1:p.Gly532=
|
|
|
NM_001278915.2:c.1686T>C
(ELN)
|
NP_001265844.1:p.Gly562=
|
|
|
NM_001278916.2:c.1524T>C
(ELN)
|
NP_001265845.1:p.Gly508=
|
|
|
NM_001278917.2:c.1638T>C
(ELN)
|
NP_001265846.1:p.Gly546=
|
|
|
NM_001278918.2:c.1401T>C
(ELN)
|
NP_001265847.1:p.Gly467=
|
|
|
NM_001278939.2:c.1755T>C
(ELN)
|
NP_001265868.1:p.Gly585=
|
|
