ENST00000262367.10:c.4407G>T
MANE Select
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ENSP00000262367.5:p.Gly1469=
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ENST00000262367.9:c.4407G>T
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ENSP00000262367.5:p.Gly1469=
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ENST00000382070.7:c.4293G>T
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ENSP00000371502.3:p.Gly1431=
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ENST00000570939.2:c.3042G>T
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ENSP00000461002.2:p.Gly1014=
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ENST00000571763.5:n.197G>T
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ENST00000574740.1:n.228G>T
|
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ENST00000576720.1:n.3230G>T
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NM_001079846.1:c.4293G>T
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NP_001073315.1:p.Gly1431=
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NM_004380.2:c.4407G>T
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NP_004371.2:p.Gly1469=
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XM_005255124.3:c.4362G>T
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XP_005255181.1:p.Gly1454=
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XM_005255125.3:c.3990G>T
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XP_005255182.1:p.Gly1330=
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XM_006720848.2:c.4146G>T
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XP_006720911.1:p.Gly1382=
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XM_011522380.1:c.4353G>T
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XP_011520682.1:p.Gly1451=
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XM_011522381.1:c.3654G>T
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XP_011520683.1:p.Gly1218=
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XM_005255124.4:c.4362G>T
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XP_005255181.1:p.Gly1454=
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XM_005255125.4:c.3990G>T
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XP_005255182.1:p.Gly1330=
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XM_006720848.3:c.4146G>T
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XP_006720911.1:p.Gly1382=
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XM_011522381.2:c.3654G>T
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XP_011520683.1:p.Gly1218=
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XM_017022944.1:c.4401G>T
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XP_016878433.1:p.Gly1467=
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NM_004380.3:c.4407G>T
MANE Select
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NP_004371.2:p.Gly1469=
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