ENST00000395796.8:c.*666G>C
|
ENSP00000379142.4:n.*666G>C
|
|
ENST00000616242.5:c.668G>C
|
ENSP00000482149.2:p.Gly223Ala
|
|
ENST00000682635.1:n.1154G>C
|
|
|
ENST00000345378.7:c.671G>C
|
ENSP00000223366.2:p.Gly224Ala
|
|
ENST00000403799.8:c.668G>C
MANE Select
|
ENSP00000384247.3:p.Gly223Ala
|
|
ENST00000671824.1:c.668G>C
|
ENSP00000500264.1:p.Gly223Ala
|
|
ENST00000673284.1:c.668G>C
|
ENSP00000499852.1:p.Gly223Ala
|
|
ENST00000345378.6:c.671G>C
|
ENSP00000223366.2:p.Gly224Ala
|
|
ENST00000395796.7:c.665G>C
|
ENSP00000379142.3:p.Gly222Ala
|
|
ENST00000403799.7:c.668G>C
|
ENSP00000384247.3:p.Gly223Ala
|
|
ENST00000437084.1:c.617G>C
|
ENSP00000402840.1:p.Gly206Ala
|
|
ENST00000616242.4:c.665G>C
|
ENSP00000482149.1:p.Gly222Ala
|
|
NM_000162.3:c.668G>C
|
NP_000153.1:p.Gly223Ala
|
|
NM_033507.1:c.671G>C
|
NP_277042.1:p.Gly224Ala
|
|
NM_033508.1:c.665G>C
|
NP_277043.1:p.Gly222Ala
|
|
XR_927223.1:n.286C>G
|
|
|
NM_000162.4:c.668G>C
|
NP_000153.1:p.Gly223Ala
|
|
NM_001354800.1:c.668G>C
|
NP_001341729.1:p.Gly223Ala
|
|
NM_033507.2:c.671G>C
|
NP_277042.1:p.Gly224Ala
|
|
NM_033508.2:c.665G>C
|
NP_277043.1:p.Gly222Ala
|
|
XR_927223.2:n.286C>G
|
|
|
NM_000162.5:c.668G>C
MANE Select
|
NP_000153.1:p.Gly223Ala
|
|
NM_033507.3:c.671G>C
|
NP_277042.1:p.Gly224Ala
|
|
NM_033508.3:c.665G>C
|
NP_277043.1:p.Gly222Ala
|
|