ENST00000337653.7:c.824G>T
MANE Select
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ENSP00000337103.2:p.Gly275Val
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ENST00000337653.6:c.824G>T
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ENSP00000337103.2:p.Gly275Val
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ENST00000339797.5:c.470G>T
|
ENSP00000343486.1:p.Gly157Val
|
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ENST00000351556.7:c.470G>T
|
ENSP00000345878.3:p.Gly157Val
|
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ENST00000395559.6:c.470G>T
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ENSP00000378926.2:p.Gly157Val
|
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ENST00000395562.2:c.578G>T
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ENSP00000378929.2:p.Gly193Val
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ENST00000466590.6:c.*555G>T
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ENSP00000473443.1:n.*555G>T
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NM_001142929.1:c.470G>T
|
NP_001136401.1:p.Gly157Val
|
|
NM_001142933.1:c.578G>T
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NP_001136405.1:p.Gly193Val
|
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NM_001142934.1:c.470G>T
|
NP_001136406.1:p.Gly157Val
|
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NM_020549.4:c.824G>T
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NP_065574.3:p.Gly275Val
|
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NM_020984.3:c.470G>T
|
NP_066264.3:p.Gly157Val
|
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NM_020985.3:c.470G>T
|
NP_066265.3:p.Gly157Val
|
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NM_020986.3:c.470G>T
|
NP_066266.3:p.Gly157Val
|
|
NM_001142929.2:c.470G>T
|
NP_001136401.2:p.Gly157Val
|
|
NM_001142933.2:c.578G>T
|
NP_001136405.2:p.Gly193Val
|
|
NM_001142934.2:c.470G>T
|
NP_001136406.2:p.Gly157Val
|
|
NM_020549.5:c.824G>T
MANE Select
|
NP_065574.4:p.Gly275Val
|
|
NM_020984.4:c.470G>T
|
NP_066264.4:p.Gly157Val
|
|
NM_020985.4:c.470G>T
|
NP_066265.4:p.Gly157Val
|
|
NM_020986.4:c.470G>T
|
NP_066266.4:p.Gly157Val
|
|