ENST00000299506.3:c.108G>A
MANE Select
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ENSP00000299506.3:p.Gln36=
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ENST00000299506.2:c.108G>A
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ENSP00000299506.2:p.Gln36=
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|
ENST00000305253.8:c.273G>A
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ENSP00000305426.4:p.Gln91=
|
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ENST00000534099.5:c.126G>A
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ENSP00000434400.1:p.Gln42=
|
|
NM_003320.4:c.273G>A
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NP_003311.2:p.Gln91=
|
|
NM_177972.2:c.108G>A
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NP_813977.1:p.Gln36=
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|
XM_005253109.2:c.234G>A
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XP_005253166.1:p.Gln78=
|
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XM_011520344.1:c.144G>A
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XP_011518646.1:p.Gln48=
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|
XM_005253109.3:c.234G>A
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XP_005253166.1:p.Gln78=
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|
XM_011520344.2:c.144G>A
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XP_011518646.1:p.Gln48=
|
|
NM_177972.3:c.108G>A
MANE Select
|
NP_813977.1:p.Gln36=
|
|
NM_003320.5:c.273G>A
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NP_003311.2:p.Gln91=
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