ENST00000328195.8:c.408T=
MANE Select
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ENSP00000333551.3:p.Pro136=
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ENST00000328195.7:c.408T=
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ENSP00000333551.3:p.Pro136=
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ENST00000518036.5:c.*260T=
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ENSP00000428005.1:n.*260T=
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ENST00000521631.1:n.91T=
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ENST00000523187.5:c.252T=
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ENSP00000427886.1:p.Pro84=
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ENST00000523358.5:c.408T=
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ENSP00000427778.1:p.Pro136=
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ENST00000523521.1:c.165T=
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ENSP00000429425.1:p.Pro55=
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NM_007198.3:c.408T=
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NP_009129.1:p.Pro136=
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NM_001349346.1:c.408T=
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NP_001336275.1:p.Pro136=
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NM_001349347.1:c.402T=
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NP_001336276.1:p.Pro134=
|
|
NM_001349348.1:c.252T=
|
NP_001336277.1:p.Pro84=
|
|
NM_007198.4:c.408T=
MANE Select
|
NP_009129.1:p.Pro136=
|
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NM_001349346.2:c.408T=
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NP_001336275.1:p.Pro136=
|
|
NM_001349347.2:c.402T=
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NP_001336276.1:p.Pro134=
|
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NM_001349348.2:c.252T=
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NP_001336277.1:p.Pro84=
|
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