ENST00000426263.10:c.423C=
MANE Select
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ENSP00000416293.2:p.Pro141=
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ENST00000674765.1:c.423C=
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ENSP00000501811.1:p.Pro141=
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ENST00000675112.1:n.446C=
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ENST00000676254.1:n.872C=
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ENST00000372500.4:c.327C=
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ENSP00000361578.4:p.Pro109=
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ENST00000426263.7:c.423C=
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ENSP00000416293.2:p.Pro141=
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ENST00000439722.2:c.302C=
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ENSP00000395521.2:n.302C=
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ENST00000475162.3:c.322C=
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ENST00000625233.2:n.631C=
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|
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ENST00000630287.2:c.423C=
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ENSP00000486694.1:p.Pro141=
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NM_006516.2:c.423C=
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NP_006507.2:p.Pro141=
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|
NM_006516.3:c.423C=
|
NP_006507.2:p.Pro141=
|
|
NM_006516.4:c.423C=
MANE Select
|
NP_006507.2:p.Pro141=
|
|