|
ENST00000707132.1:n.2168G>T
|
|
|
|
ENST00000707133.1:n.598G>T
|
|
|
|
ENST00000707134.1:n.867G>T
|
|
|
|
ENST00000346798.8:c.2201G>T
MANE Select
|
ENSP00000284981.4:p.Gly734Val
|
|
|
ENST00000346798.7:c.2201G>T
|
ENSP00000284981.4:p.Gly734Val
|
|
|
ENST00000348990.9:c.1976G>T
|
ENSP00000345463.5:p.Gly659Val
|
|
|
ENST00000354192.7:c.1808G>T
|
ENSP00000346129.3:p.Gly603Val
|
|
|
ENST00000357903.7:c.2144G>T
|
ENSP00000350578.3:p.Gly715Val
|
|
|
ENST00000358918.7:c.2147G>T
|
ENSP00000351796.3:p.Gly716Val
|
|
|
ENST00000359726.7:c.1871G>T
|
ENSP00000352760.4:p.Gly624Val
|
|
|
ENST00000439274.6:c.2033G>T
|
ENSP00000398879.2:p.Gly678Val
|
|
|
ENST00000440126.7:c.2129G>T
|
ENSP00000387483.2:p.Gly710Val
|
|
|
ENST00000464867.1:n.548G>T
|
|
|
|
NM_000484.3:c.2201G>T
|
NP_000475.1:p.Gly734Val
|
|
|
NM_001136016.3:c.2129G>T
|
NP_001129488.1:p.Gly710Val
|
|
|
NM_001136129.2:c.1808G>T
|
NP_001129601.1:p.Gly603Val
|
|
|
NM_001136130.2:c.2033G>T
|
NP_001129602.1:p.Gly678Val
|
|
|
NM_001136131.2:c.1871G>T
|
NP_001129603.1:p.Gly624Val
|
|
|
NM_001204301.1:c.2147G>T
|
NP_001191230.1:p.Gly716Val
|
|
|
NM_001204302.1:c.2090G>T
|
NP_001191231.1:p.Gly697Val
|
|
|
NM_001204303.1:c.1922G>T
|
NP_001191232.1:p.Gly641Val
|
|
|
NM_201413.2:c.2144G>T
|
NP_958816.1:p.Gly715Val
|
|
|
NM_201414.2:c.1976G>T
|
NP_958817.1:p.Gly659Val
|
|
|
NM_000484.4:c.2201G>T
MANE Select
|
NP_000475.1:p.Gly734Val
|
|
|
NM_001136129.3:c.1808G>T
|
NP_001129601.1:p.Gly603Val
|
|
|
NM_001136130.3:c.2033G>T
|
NP_001129602.1:p.Gly678Val
|
|
|
NM_001204301.2:c.2147G>T
|
NP_001191230.1:p.Gly716Val
|
|
|
NM_001204302.2:c.2090G>T
|
NP_001191231.1:p.Gly697Val
|
|
|
NM_001204303.2:c.1922G>T
|
NP_001191232.1:p.Gly641Val
|
|
|
NM_201413.3:c.2144G>T
|
NP_958816.1:p.Gly715Val
|
|
|
NM_201414.3:c.1976G>T
|
NP_958817.1:p.Gly659Val
|
|
|
NM_001136131.3:c.1871G>T
|
NP_001129603.1:p.Gly624Val
|
|
|
NM_001385253.1:c.2033G>T
|
NP_001372182.1:p.Gly678Val
|
|
