ENST00000262367.10:c.6926G>T
MANE Select
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ENSP00000262367.5:p.Gly2309Val
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ENST00000262367.9:c.6926G>T
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ENSP00000262367.5:p.Gly2309Val
|
|
ENST00000382070.7:c.6812G>T
|
ENSP00000371502.3:p.Gly2271Val
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NM_001079846.1:c.6812G>T
|
NP_001073315.1:p.Gly2271Val
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NM_004380.2:c.6926G>T
|
NP_004371.2:p.Gly2309Val
|
|
XM_005255124.3:c.6881G>T
|
XP_005255181.1:p.Gly2294Val
|
|
XM_005255125.3:c.6509G>T
|
XP_005255182.1:p.Gly2170Val
|
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XM_006720848.2:c.6665G>T
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XP_006720911.1:p.Gly2222Val
|
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XM_011522380.1:c.6872G>T
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XP_011520682.1:p.Gly2291Val
|
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XM_011522381.1:c.6173G>T
|
XP_011520683.1:p.Gly2058Val
|
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XM_005255124.4:c.6881G>T
|
XP_005255181.1:p.Gly2294Val
|
|
XM_005255125.4:c.6509G>T
|
XP_005255182.1:p.Gly2170Val
|
|
XM_006720848.3:c.6665G>T
|
XP_006720911.1:p.Gly2222Val
|
|
XM_011522381.2:c.6173G>T
|
XP_011520683.1:p.Gly2058Val
|
|
XM_017022944.1:c.6920G>T
|
XP_016878433.1:p.Gly2307Val
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|
NM_004380.3:c.6926G>T
MANE Select
|
NP_004371.2:p.Gly2309Val
|
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