ENST00000592092.2:n.695G>C
|
|
|
ENST00000673918.2:c.6323G>C
|
ENSP00000501283.1:p.Gly2108Ala
|
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ENST00000674114.2:c.3930G>C
|
ENSP00000501039.2:n.3930G>C
|
|
ENST00000684977.1:c.1607G>C
|
ENSP00000509384.1:p.Gly536Ala
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ENST00000689544.1:n.1542G>C
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|
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ENST00000691421.1:c.1610G>C
|
ENSP00000508674.1:p.Gly537Ala
|
|
ENST00000691855.1:c.5931G>C
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|
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ENST00000692961.1:c.6389G>C
|
ENSP00000509289.1:p.Gly2130Ala
|
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ENST00000693677.1:c.704+609G>C
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ENSP00000509779.1:n.704+609G>C
|
|
ENST00000420124.4:c.6389G>C
MANE Select
|
ENSP00000398837.2:p.Gly2130Ala
|
|
ENST00000673918.1:c.6323G>C
|
ENSP00000501283.1:p.Gly2108Ala
|
|
ENST00000674114.1:c.3711G>C
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|
|
ENST00000420124.2:c.6389G>C
|
ENSP00000398837.1:p.Gly2130Ala
|
|
NM_014727.2:c.6389G>C
|
NP_055542.1:p.Gly2130Ala
|
|
XM_011527561.1:c.6323G>C
|
XP_011525863.1:p.Gly2108Ala
|
|
XM_011527562.1:c.6389G>C
|
XP_011525864.1:p.Gly2130Ala
|
|
XM_011527563.1:c.6113G>C
|
XP_011525865.1:p.Gly2038Ala
|
|
XM_011527561.2:c.5825G>C
|
XP_011525863.2:p.Gly1942Ala
|
|
XM_011527562.2:c.6389G>C
|
XP_011525864.1:p.Gly2130Ala
|
|
XM_017027544.1:c.6389G>C
|
XP_016883033.1:p.Gly2130Ala
|
|
XM_017027545.1:c.5825G>C
|
XP_016883034.1:p.Gly1942Ala
|
|
XM_017027546.1:c.3353G>C
|
XP_016883035.1:p.Gly1118Ala
|
|
NM_014727.3:c.6389G>C
MANE Select
|
NP_055542.1:p.Gly2130Ala
|
|