ENST00000221930.6:c.887G>T
MANE Select
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ENSP00000221930.4:p.Arg296Leu
|
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ENST00000600196.2:c.739G>T
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ENSP00000504008.1:p.Gly247Cys
|
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ENST00000677934.1:c.661G>T
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ENSP00000504769.1:p.Gly221Cys
|
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ENST00000221930.5:c.887G>T
|
ENSP00000221930.4:p.Arg296Leu
|
|
ENST00000598758.5:c.175G>T
|
|
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ENST00000600196.1:n.199G>T
|
|
|
NM_000660.5:c.887G>T
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NP_000651.3:p.Arg296Leu
|
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XM_011527242.1:c.890G>T
|
XP_011525544.1:p.Arg297Leu
|
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NM_000660.6:c.887G>T
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NP_000651.3:p.Arg296Leu
|
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XM_011527242.2:c.890G>T
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XP_011525544.1:p.Arg297Leu
|
|
NM_000660.7:c.887G>T
MANE Select
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NP_000651.3:p.Arg296Leu
|
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