ENST00000592092.2:n.302G>C
|
|
|
ENST00000673918.2:c.5930G>C
|
ENSP00000501283.1:p.Gly1977Ala
|
|
ENST00000674114.2:c.3537G>C
|
ENSP00000501039.2:n.3537G>C
|
|
ENST00000684977.1:c.1214G>C
|
ENSP00000509384.1:p.Gly405Ala
|
|
ENST00000689544.1:n.1149G>C
|
|
|
ENST00000691421.1:c.1217G>C
|
ENSP00000508674.1:p.Gly406Ala
|
|
ENST00000691855.1:c.5538G>C
|
|
|
ENST00000692961.1:c.5996G>C
|
ENSP00000509289.1:p.Gly1999Ala
|
|
ENST00000693677.1:c.704+216G>C
|
ENSP00000509779.1:n.704+216G>C
|
|
ENST00000420124.4:c.5996G>C
MANE Select
|
ENSP00000398837.2:p.Gly1999Ala
|
|
ENST00000673918.1:c.5930G>C
|
ENSP00000501283.1:p.Gly1977Ala
|
|
ENST00000674114.1:c.3318G>C
|
|
|
ENST00000420124.2:c.5996G>C
|
ENSP00000398837.1:p.Gly1999Ala
|
|
NM_014727.2:c.5996G>C
|
NP_055542.1:p.Gly1999Ala
|
|
XM_011527561.1:c.5930G>C
|
XP_011525863.1:p.Gly1977Ala
|
|
XM_011527562.1:c.5996G>C
|
XP_011525864.1:p.Gly1999Ala
|
|
XM_011527563.1:c.5720G>C
|
XP_011525865.1:p.Gly1907Ala
|
|
XM_011527561.2:c.5432G>C
|
XP_011525863.2:p.Gly1811Ala
|
|
XM_011527562.2:c.5996G>C
|
XP_011525864.1:p.Gly1999Ala
|
|
XM_017027544.1:c.5996G>C
|
XP_016883033.1:p.Gly1999Ala
|
|
XM_017027545.1:c.5432G>C
|
XP_016883034.1:p.Gly1811Ala
|
|
XM_017027546.1:c.2960G>C
|
XP_016883035.1:p.Gly987Ala
|
|
NM_014727.3:c.5996G>C
MANE Select
|
NP_055542.1:p.Gly1999Ala
|
|