ENST00000592092.2:n.734C>G
|
|
|
ENST00000673918.2:c.6362C>G
|
ENSP00000501283.1:p.Ala2121Gly
|
|
ENST00000674114.2:c.3969C>G
|
ENSP00000501039.2:n.3969C>G
|
|
ENST00000684977.1:c.1646C>G
|
ENSP00000509384.1:p.Ala549Gly
|
|
ENST00000689544.1:n.1581C>G
|
|
|
ENST00000691421.1:c.1649C>G
|
ENSP00000508674.1:p.Ala550Gly
|
|
ENST00000691855.1:c.5970C>G
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|
|
ENST00000692961.1:c.6428C>G
|
ENSP00000509289.1:p.Ala2143Gly
|
|
ENST00000693677.1:c.705-620C>G
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ENSP00000509779.1:n.705-620C>G
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|
ENST00000420124.4:c.6428C>G
MANE Select
|
ENSP00000398837.2:p.Ala2143Gly
|
|
ENST00000673918.1:c.6362C>G
|
ENSP00000501283.1:p.Ala2121Gly
|
|
ENST00000674114.1:c.3750C>G
|
|
|
ENST00000420124.2:c.6428C>G
|
ENSP00000398837.1:p.Ala2143Gly
|
|
NM_014727.2:c.6428C>G
|
NP_055542.1:p.Ala2143Gly
|
|
XM_011527561.1:c.6362C>G
|
XP_011525863.1:p.Ala2121Gly
|
|
XM_011527562.1:c.6428C>G
|
XP_011525864.1:p.Ala2143Gly
|
|
XM_011527563.1:c.6152C>G
|
XP_011525865.1:p.Ala2051Gly
|
|
XM_011527561.2:c.5864C>G
|
XP_011525863.2:p.Ala1955Gly
|
|
XM_011527562.2:c.6428C>G
|
XP_011525864.1:p.Ala2143Gly
|
|
XM_017027544.1:c.6428C>G
|
XP_016883033.1:p.Ala2143Gly
|
|
XM_017027545.1:c.5864C>G
|
XP_016883034.1:p.Ala1955Gly
|
|
XM_017027546.1:c.3392C>G
|
XP_016883035.1:p.Ala1131Gly
|
|
NM_014727.3:c.6428C>G
MANE Select
|
NP_055542.1:p.Ala2143Gly
|
|