ENST00000355832.10:c.3580G>T
MANE Select
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ENSP00000348089.5:p.Glu1194Ter
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ENST00000679552.1:n.651G>T
|
|
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ENST00000679871.1:n.726G>T
|
|
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ENST00000679974.1:n.629G>T
|
|
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ENST00000681632.1:n.4983G>T
|
|
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ENST00000681659.1:c.3421G>T
|
ENSP00000505631.1:p.Glu1141Ter
|
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ENST00000355832.9:c.3580G>T
|
ENSP00000348089.5:p.Glu1194Ter
|
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ENST00000623073.3:c.*1876G>T
|
ENSP00000485650.1:n.*1876G>T
|
|
ENST00000623115.3:c.1690G>T
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ENSP00000485321.1:p.Glu564Ter
|
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ENST00000624341.3:c.1412G>T
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|
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NM_000124.3:c.3580G>T
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NP_000115.1:p.Glu1194Ter
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XR_945953.1:n.243-1185C>A
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|
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NM_001346440.1:c.3580G>T
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NP_001333369.1:p.Glu1194Ter
|
|
NM_000124.4:c.3580G>T
MANE Select
|
NP_000115.1:p.Glu1194Ter
|
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NM_001346440.2:c.3580G>T
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NP_001333369.1:p.Glu1194Ter
|
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