ENST00000426263.10:c.1144G>C
MANE Select
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ENSP00000416293.2:p.Gly382Arg
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ENST00000674545.1:n.1761G>C
|
|
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ENST00000674765.1:c.1030-882G>C
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ENSP00000501811.1:n.1030-882G>C
|
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ENST00000675112.1:n.1445G>C
|
|
|
ENST00000676254.1:n.1593G>C
|
|
|
ENST00000426263.7:c.1144G>C
|
ENSP00000416293.2:p.Gly382Arg
|
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ENST00000475162.3:c.416-761G>C
|
|
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ENST00000630287.2:c.*459G>C
|
ENSP00000486694.1:n.*459G>C
|
|
NM_006516.2:c.1144G>C
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NP_006507.2:p.Gly382Arg
|
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NM_006516.3:c.1144G>C
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NP_006507.2:p.Gly382Arg
|
|
NM_006516.4:c.1144G>C
MANE Select
|
NP_006507.2:p.Gly382Arg
|
|