ENST00000592092.2:n.605G>C
|
|
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ENST00000673918.2:c.6233G>C
|
ENSP00000501283.1:p.Gly2078Ala
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ENST00000674114.2:c.3840G>C
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ENSP00000501039.2:n.3840G>C
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ENST00000684977.1:c.1517G>C
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ENSP00000509384.1:p.Gly506Ala
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ENST00000689544.1:n.1452G>C
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|
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ENST00000691421.1:c.1520G>C
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ENSP00000508674.1:p.Gly507Ala
|
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ENST00000691855.1:c.5841G>C
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|
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ENST00000692961.1:c.6299G>C
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ENSP00000509289.1:p.Gly2100Ala
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ENST00000693677.1:c.704+519G>C
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ENSP00000509779.1:n.704+519G>C
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ENST00000420124.4:c.6299G>C
MANE Select
|
ENSP00000398837.2:p.Gly2100Ala
|
|
ENST00000673918.1:c.6233G>C
|
ENSP00000501283.1:p.Gly2078Ala
|
|
ENST00000674114.1:c.3621G>C
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|
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ENST00000420124.2:c.6299G>C
|
ENSP00000398837.1:p.Gly2100Ala
|
|
NM_014727.2:c.6299G>C
|
NP_055542.1:p.Gly2100Ala
|
|
XM_011527561.1:c.6233G>C
|
XP_011525863.1:p.Gly2078Ala
|
|
XM_011527562.1:c.6299G>C
|
XP_011525864.1:p.Gly2100Ala
|
|
XM_011527563.1:c.6023G>C
|
XP_011525865.1:p.Gly2008Ala
|
|
XM_011527561.2:c.5735G>C
|
XP_011525863.2:p.Gly1912Ala
|
|
XM_011527562.2:c.6299G>C
|
XP_011525864.1:p.Gly2100Ala
|
|
XM_017027544.1:c.6299G>C
|
XP_016883033.1:p.Gly2100Ala
|
|
XM_017027545.1:c.5735G>C
|
XP_016883034.1:p.Gly1912Ala
|
|
XM_017027546.1:c.3263G>C
|
XP_016883035.1:p.Gly1088Ala
|
|
NM_014727.3:c.6299G>C
MANE Select
|
NP_055542.1:p.Gly2100Ala
|
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