ENST00000706989.1:c.2328C>T
|
ENSP00000516702.1:p.Gly776=
|
|
ENST00000359125.7:c.2274C>T
MANE Select
|
ENSP00000352035.2:p.Gly758=
|
|
ENST00000637193.1:c.1671C>T
|
ENSP00000490734.1:p.Gly557=
|
|
ENST00000344462.8:c.2181C>T
|
ENSP00000339611.4:p.Gly727=
|
|
ENST00000357249.6:c.1842C>T
|
ENSP00000349789.3:p.Gly614=
|
|
ENST00000359125.6:c.2274C>T
|
ENSP00000352035.2:p.Gly758=
|
|
ENST00000360480.7:c.2190C>T
|
ENSP00000353668.3:p.Gly730=
|
|
ENST00000370224.5:c.2241+57C>T
|
ENSP00000359244.2:n.2241+57C>T
|
|
ENST00000625514.2:c.2205+57C>T
|
ENSP00000486040.1:n.2205+57C>T
|
|
ENST00000626839.2:c.2220C>T
|
ENSP00000486706.1:p.Gly740=
|
|
ENST00000629241.2:c.2133+57C>T
|
ENSP00000487142.1:n.2133+57C>T
|
|
ENST00000629676.2:c.1680-6146C>T
|
ENSP00000486194.1:n.1680-6146C>T
|
|
NM_004518.4:c.2190C>T
|
NP_004509.2:p.Gly730=
|
|
NM_172106.1:c.2220C>T
|
NP_742104.1:p.Gly740=
|
|
NM_172107.2:c.2274C>T
|
NP_742105.1:p.Gly758=
|
|
NM_172108.3:c.2181C>T
|
NP_742106.1:p.Gly727=
|
|
XM_006723787.1:c.2316C>T
|
XP_006723850.1:p.Gly772=
|
|
XM_011528807.1:c.2382C>T
|
XP_011527109.1:p.Gly794=
|
|
XM_011528808.1:c.2379C>T
|
XP_011527110.1:p.Gly793=
|
|
XM_011528809.1:c.2352C>T
|
XP_011527111.1:p.Gly784=
|
|
XM_011528810.1:c.2328C>T
|
XP_011527112.1:p.Gly776=
|
|
XM_011528811.1:c.2298C>T
|
XP_011527113.1:p.Gly766=
|
|
XM_011528812.1:c.2271C>T
|
XP_011527114.1:p.Gly757=
|
|
XM_011528813.1:c.2256C>T
|
XP_011527115.1:p.Gly752=
|
|
XM_011528814.1:c.1863C>T
|
XP_011527116.1:p.Gly621=
|
|
NM_004518.5:c.2190C>T
|
NP_004509.2:p.Gly730=
|
|
NM_172106.2:c.2220C>T
|
NP_742104.1:p.Gly740=
|
|
NM_172107.3:c.2274C>T
|
NP_742105.1:p.Gly758=
|
|
NM_172108.4:c.2181C>T
|
NP_742106.1:p.Gly727=
|
|
XM_011528810.2:c.2328C>T
|
XP_011527112.1:p.Gly776=
|
|
XM_011528811.2:c.2298C>T
|
XP_011527113.1:p.Gly766=
|
|
XM_017027841.2:c.2325C>T
|
XP_016883330.1:p.Gly775=
|
|
XM_017027842.2:c.2262C>T
|
XP_016883331.1:p.Gly754=
|
|
XM_017027843.1:c.2259C>T
|
XP_016883332.1:p.Gly753=
|
|
XM_017027844.2:c.2217C>T
|
XP_016883333.1:p.Gly739=
|
|
XM_017027845.1:c.1290C>T
|
XP_016883334.1:p.Gly430=
|
|
NM_004518.6:c.2190C>T
|
NP_004509.2:p.Gly730=
|
|
NM_172106.3:c.2220C>T
|
NP_742104.1:p.Gly740=
|
|
NM_172107.4:c.2274C>T
MANE Select
|
NP_742105.1:p.Gly758=
|
|
NM_172108.5:c.2181C>T
|
NP_742106.1:p.Gly727=
|
|
NM_001382235.1:c.2328C>T
|
NP_001369164.1:p.Gly776=
|
|