ENST00000262367.10:c.3320A>G
MANE Select
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ENSP00000262367.5:p.Glu1107Gly
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ENST00000262367.9:c.3320A>G
|
ENSP00000262367.5:p.Glu1107Gly
|
|
ENST00000382070.7:c.3206A>G
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ENSP00000371502.3:p.Glu1069Gly
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ENST00000570939.2:c.1925A>G
|
ENSP00000461002.2:p.Glu642Gly
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NM_001079846.1:c.3206A>G
|
NP_001073315.1:p.Glu1069Gly
|
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NM_004380.2:c.3320A>G
|
NP_004371.2:p.Glu1107Gly
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XM_005255124.3:c.3275A>G
|
XP_005255181.1:p.Glu1092Gly
|
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XM_005255125.3:c.2903A>G
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XP_005255182.1:p.Glu968Gly
|
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XM_006720848.2:c.3320A>G
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XP_006720911.1:p.Glu1107Gly
|
|
XM_011522380.1:c.3266A>G
|
XP_011520682.1:p.Glu1089Gly
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XM_011522381.1:c.2567A>G
|
XP_011520683.1:p.Glu856Gly
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XM_011522382.1:c.3320A>G
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XP_011520684.1:p.Glu1107Gly
|
|
XM_005255124.4:c.3275A>G
|
XP_005255181.1:p.Glu1092Gly
|
|
XM_005255125.4:c.2903A>G
|
XP_005255182.1:p.Glu968Gly
|
|
XM_006720848.3:c.3320A>G
|
XP_006720911.1:p.Glu1107Gly
|
|
XM_011522381.2:c.2567A>G
|
XP_011520683.1:p.Glu856Gly
|
|
XM_011522382.3:c.3320A>G
|
XP_011520684.1:p.Glu1107Gly
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|
XM_017022944.1:c.3314A>G
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XP_016878433.1:p.Glu1105Gly
|
|
NM_004380.3:c.3320A>G
MANE Select
|
NP_004371.2:p.Glu1107Gly
|
|