ENST00000651671.1:c.6132A>T
MANE Select
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ENSP00000498587.1:p.Ala2044=
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ENST00000679595.1:c.*1172A>T
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ENSP00000506241.1:n.*1172A>T
|
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ENST00000679969.1:n.2728A>T
|
|
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ENST00000680003.1:n.2464A>T
|
|
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ENST00000680133.1:c.6018A>T
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ENSP00000505319.1:p.Ala2006=
|
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ENST00000680218.1:c.6012A>T
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ENSP00000505339.1:p.Ala2004=
|
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ENST00000680668.1:c.6018A>T
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ENSP00000506336.1:p.Ala2006=
|
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ENST00000680778.1:c.3729A>T
|
ENSP00000506033.1:p.Ala1243=
|
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ENST00000680924.1:c.*3532A>T
|
ENSP00000506031.1:n.*3532A>T
|
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ENST00000681135.1:c.*3741A>T
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ENSP00000506636.1:n.*3741A>T
|
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ENST00000681298.1:n.4237A>T
|
|
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ENST00000681454.1:c.*5368A>T
|
ENSP00000505763.1:n.*5368A>T
|
|
ENST00000277541.6:c.6132A>T
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ENSP00000277541.6:p.Ala2044=
|
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NM_017617.3:c.6132A>T
|
NP_060087.3:p.Ala2044=
|
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XM_011518717.1:c.5433A>T
|
XP_011517019.1:p.Ala1811=
|
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NM_017617.5:c.6132A>T
MANE Select
|
NP_060087.3:p.Ala2044=
|
|
XM_011518717.2:c.5409A>T
|
XP_011517019.2:p.Ala1803=
|
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