ENST00000282516.13:c.6804T>G
MANE Select
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ENSP00000282516.8:p.Gly2268=
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ENST00000652901.1:c.6804T>G
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ENSP00000499536.1:p.Gly2268=
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ENST00000282516.12:c.6804T>G
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ENSP00000282516.8:p.Gly2268=
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ENST00000448238.2:c.6804T>G
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ENSP00000406266.2:p.Gly2268=
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ENST00000621733.1:c.1-15427T>G
|
ENSP00000480694.1:n.1-15427T>G
|
|
NM_015384.4:c.6804T>G
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NP_056199.2:p.Gly2268=
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NM_133433.3:c.6804T>G
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NP_597677.2:p.Gly2268=
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XM_005248280.2:c.6804T>G
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XP_005248337.1:p.Gly2268=
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XM_005248282.3:c.6060T>G
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XP_005248339.2:p.Gly2020=
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|
XM_006714467.2:c.6804T>G
|
XP_006714530.1:p.Gly2268=
|
|
XM_006714468.1:c.6606T>G
|
XP_006714531.1:p.Gly2202=
|
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XM_011514014.1:c.6423T>G
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XP_011512316.1:p.Gly2141=
|
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XM_011514015.1:c.6804T>G
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XP_011512317.1:p.Gly2268=
|
|
XM_005248280.3:c.6804T>G
|
XP_005248337.1:p.Gly2268=
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XM_005248282.5:c.6144T>G
|
XP_005248339.3:p.Gly2048=
|
|
XM_006714468.2:c.6606T>G
|
XP_006714531.1:p.Gly2202=
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XM_017009329.1:c.6804T>G
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XP_016864818.1:p.Gly2268=
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XM_017009330.2:c.5187T>G
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XP_016864819.1:p.Gly1729=
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XM_017009331.1:c.5178T>G
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XP_016864820.1:p.Gly1726=
|
|
NM_133433.4:c.6804T>G
MANE Select
|
NP_597677.2:p.Gly2268=
|
|
NM_015384.5:c.6804T>G
|
NP_056199.2:p.Gly2268=
|
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