ENST00000366647.9:c.641G=
MANE Select
|
ENSP00000355607.4:p.Gly214=
|
|
ENST00000644483.1:c.*327G=
|
ENSP00000496537.1:n.*327G=
|
|
ENST00000366647.8:c.641G=
|
ENSP00000355607.4:p.Gly214=
|
|
ENST00000416000.1:c.611G=
|
ENSP00000411640.1:p.Gly204=
|
|
ENST00000436239.5:c.458G=
|
ENSP00000402811.1:p.Gly153=
|
|
NM_001316350.1:c.458G=
|
NP_001303279.1:p.Gly153=
|
|
NM_014236.3:c.641G=
|
NP_055051.1:p.Gly214=
|
|
XM_005273313.3:c.638G=
|
XP_005273370.1:p.Gly213=
|
|
XM_011544303.1:c.314G=
|
XP_011542605.1:p.Gly105=
|
|
XM_011544304.1:c.314G=
|
XP_011542606.1:p.Gly105=
|
|
XM_005273313.4:c.638G=
|
XP_005273370.1:p.Gly213=
|
|
XM_011544303.3:c.314G=
|
XP_011542605.1:p.Gly105=
|
|
XM_011544304.2:c.314G=
|
XP_011542606.1:p.Gly105=
|
|
NM_014236.4:c.641G=
MANE Select
|
NP_055051.1:p.Gly214=
|
|
NM_001316350.2:c.458G=
|
NP_001303279.1:p.Gly153=
|
|