ENST00000651671.1:c.6129C>G
MANE Select
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ENSP00000498587.1:p.Ala2043=
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ENST00000679595.1:c.*1169C>G
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ENSP00000506241.1:n.*1169C>G
|
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ENST00000679969.1:n.2725C>G
|
|
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ENST00000680003.1:n.2461C>G
|
|
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ENST00000680133.1:c.6015C>G
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ENSP00000505319.1:p.Ala2005=
|
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ENST00000680218.1:c.6009C>G
|
ENSP00000505339.1:p.Ala2003=
|
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ENST00000680668.1:c.6015C>G
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ENSP00000506336.1:p.Ala2005=
|
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ENST00000680778.1:c.3726C>G
|
ENSP00000506033.1:p.Ala1242=
|
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ENST00000680924.1:c.*3529C>G
|
ENSP00000506031.1:n.*3529C>G
|
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ENST00000681135.1:c.*3738C>G
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ENSP00000506636.1:n.*3738C>G
|
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ENST00000681298.1:n.4234C>G
|
|
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ENST00000681454.1:c.*5365C>G
|
ENSP00000505763.1:n.*5365C>G
|
|
ENST00000277541.6:c.6129C>G
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ENSP00000277541.6:p.Ala2043=
|
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NM_017617.3:c.6129C>G
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NP_060087.3:p.Ala2043=
|
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XM_011518717.1:c.5430C>G
|
XP_011517019.1:p.Ala1810=
|
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NM_017617.5:c.6129C>G
MANE Select
|
NP_060087.3:p.Ala2043=
|
|
XM_011518717.2:c.5406C>G
|
XP_011517019.2:p.Ala1802=
|
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