ENST00000338508.9:c.2480A>G
|
ENSP00000345193.7:p.Glu827Gly
|
|
ENST00000412252.6:c.757+4257A>G
|
ENSP00000414876.2:n.757+4257A>G
|
|
ENST00000601538.6:c.4247A>G
MANE Select
|
ENSP00000469689.2:p.Glu1416Gly
|
|
ENST00000654939.1:c.1675A>G
|
|
|
ENST00000656230.1:c.3110A>G
|
ENSP00000499561.1:p.Glu1037Gly
|
|
ENST00000659264.1:c.2537A>G
|
ENSP00000499270.1:p.Glu846Gly
|
|
ENST00000338508.8:c.2483A>G
|
ENSP00000345193.6:p.Glu828Gly
|
|
ENST00000357171.7:c.718+4257A>G
|
ENSP00000349694.4:n.718+4257A>G
|
|
ENST00000409161.5:c.2459A>G
|
ENSP00000386491.1:p.Glu820Gly
|
|
ENST00000412252.5:c.755+4257A>G
|
|
|
ENST00000423696.6:c.3110A>G
|
ENSP00000394536.2:p.Glu1037Gly
|
|
ENST00000424924.5:c.2084A>G
|
ENSP00000402944.1:p.Glu695Gly
|
|
ENST00000449833.6:c.2483A>G
|
ENSP00000399423.3:p.Glu828Gly
|
|
ENST00000601538.5:c.4247A>G
|
ENSP00000469689.2:p.Glu1416Gly
|
|
NM_012309.4:c.4247A>G
|
NP_036441.2:p.Glu1416Gly
|
|
NM_133266.4:c.2483A>G
|
NP_573573.2:p.Glu828Gly
|
|
NR_110766.1:n.833+4257A>G
|
|
|
XM_005277930.2:c.4247A>G
|
XP_005277987.1:p.Glu1416Gly
|
|
XM_005277932.2:c.3110A>G
|
XP_005277989.1:p.Glu1037Gly
|
|
XM_006718478.2:c.4217A>G
|
XP_006718541.1:p.Glu1406Gly
|
|
XM_011544854.1:c.4259A>G
|
XP_011543156.1:p.Glu1420Gly
|
|
XM_011544855.1:c.4238A>G
|
XP_011543157.1:p.Glu1413Gly
|
|
XM_011544856.1:c.4232A>G
|
XP_011543158.1:p.Glu1411Gly
|
|
XM_011544857.1:c.4211A>G
|
XP_011543159.1:p.Glu1404Gly
|
|
XM_011544858.1:c.4259A>G
|
XP_011543160.1:p.Glu1420Gly
|
|
XM_011544859.1:c.3122A>G
|
XP_011543161.1:p.Glu1041Gly
|
|
XM_005277932.3:c.3110A>G
|
XP_005277989.1:p.Glu1037Gly
|
|
XM_017017387.1:c.4247A>G
|
XP_016872876.1:p.Glu1416Gly
|
|
XM_017017388.1:c.4247A>G
|
XP_016872877.1:p.Glu1416Gly
|
|
XM_017017389.1:c.4220A>G
|
XP_016872878.1:p.Glu1407Gly
|
|
XM_017017390.1:c.2537A>G
|
XP_016872879.1:p.Glu846Gly
|
|
NM_133266.5:c.2483A>G
|
NP_573573.2:p.Glu828Gly
|
|
NR_110766.2:n.834+4257A>G
|
|
|
NM_001379226.1:c.3110A>G
|
NP_001366155.1:p.Glu1037Gly
|
|
NM_012309.5:c.4247A>G
MANE Select
|
NP_036441.2:p.Glu1416Gly
|
|