|
ENST00000473665.2:n.5305G>A
|
|
|
|
ENST00000482662.2:n.3712G>A
|
|
|
|
ENST00000685865.1:n.1664G>A
|
|
|
|
ENST00000687250.1:n.1364G>A
|
|
|
|
ENST00000687995.1:n.1613G>A
|
|
|
|
ENST00000688205.1:c.*854G>A
|
ENSP00000509673.1:n.*854G>A
|
|
|
ENST00000688788.1:n.1500G>A
|
|
|
|
ENST00000689276.1:c.1192G>A
|
ENSP00000510012.1:p.Gly398Ser
|
|
|
ENST00000689576.1:c.1261G>A
|
ENSP00000508712.1:p.Gly421Ser
|
|
|
ENST00000690108.1:c.*917G>A
|
ENSP00000510617.1:n.*917G>A
|
|
|
ENST00000690468.1:c.982G>A
|
ENSP00000509078.1:p.Gly328Ser
|
|
|
ENST00000690595.1:c.586G>A
|
ENSP00000508979.1:p.Gly196Ser
|
|
|
ENST00000691348.1:c.1090G>A
|
ENSP00000509369.1:p.Gly364Ser
|
|
|
ENST00000691410.1:c.*838G>A
|
ENSP00000508479.1:n.*838G>A
|
|
|
ENST00000693287.1:c.577G>A
|
ENSP00000510264.1:p.Gly193Ser
|
|
|
ENST00000693681.1:c.574G>A
|
ENSP00000510789.1:p.Gly192Ser
|
|
|
ENST00000233838.9:c.1261G>A
MANE Select
|
ENSP00000233838.3:p.Gly421Ser
|
|
|
ENST00000233838.8:c.1261G>A
|
ENSP00000233838.3:p.Gly421Ser
|
|
|
ENST00000430215.7:c.1090G>A
|
ENSP00000408045.3:p.Gly364Ser
|
|
|
ENST00000465637.5:n.179-4961G>A
|
|
|
|
ENST00000473665.1:n.754G>A
|
|
|
|
ENST00000482662.1:n.678G>A
|
|
|
|
NM_000821.5:c.1261G>A
|
NP_000812.2:p.Gly421Ser
|
|
|
NM_000821.6:c.1261G>A
|
NP_000812.2:p.Gly421Ser
|
|
|
NM_001142269.2:c.1090G>A
|
NP_001135741.1:p.Gly364Ser
|
|
|
NM_001142269.3:c.1090G>A
|
NP_001135741.1:p.Gly364Ser
|
|
|
XM_005264259.3:c.1261G>A
|
XP_005264316.1:p.Gly421Ser
|
|
|
XM_011532764.1:c.439G>A
|
XP_011531066.1:p.Gly147Ser
|
|
|
XM_011532765.1:c.439G>A
|
XP_011531067.1:p.Gly147Ser
|
|
|
XR_939677.1:n.1326G>A
|
|
|
|
XM_005264259.5:c.1261G>A
|
XP_005264316.1:p.Gly421Ser
|
|
|
XM_011532764.3:c.439G>A
|
XP_011531066.1:p.Gly147Ser
|
|
|
XM_011532765.3:c.439G>A
|
XP_011531067.1:p.Gly147Ser
|
|
|
XM_017003803.2:c.1090G>A
|
XP_016859292.1:p.Gly364Ser
|
|
|
XR_001738703.2:n.1326G>A
|
|
|
|
NM_000821.7:c.1261G>A
MANE Select
|
NP_000812.2:p.Gly421Ser
|
|
|
NM_001142269.4:c.1090G>A
|
NP_001135741.1:p.Gly364Ser
|
|
