ENST00000366647.9:c.579A>T
MANE Select
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ENSP00000355607.4:p.Gly193=
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ENST00000644483.1:c.*265A>T
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ENSP00000496537.1:n.*265A>T
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ENST00000366647.8:c.579A>T
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ENSP00000355607.4:p.Gly193=
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ENST00000416000.1:c.549A>T
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ENSP00000411640.1:p.Gly183=
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ENST00000436239.5:c.396A>T
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ENSP00000402811.1:p.Gly132=
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NM_001316350.1:c.396A>T
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NP_001303279.1:p.Gly132=
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NM_014236.3:c.579A>T
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NP_055051.1:p.Gly193=
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XM_005273313.3:c.576A>T
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XP_005273370.1:p.Gly192=
|
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XM_011544303.1:c.252A>T
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XP_011542605.1:p.Gly84=
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XM_011544304.1:c.252A>T
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XP_011542606.1:p.Gly84=
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XM_005273313.4:c.576A>T
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XP_005273370.1:p.Gly192=
|
|
XM_011544303.3:c.252A>T
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XP_011542605.1:p.Gly84=
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XM_011544304.2:c.252A>T
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XP_011542606.1:p.Gly84=
|
|
NM_014236.4:c.579A>T
MANE Select
|
NP_055051.1:p.Gly193=
|
|
NM_001316350.2:c.396A>T
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NP_001303279.1:p.Gly132=
|
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