ENST00000357749.7:c.814G>T
MANE Select
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ENSP00000350386.2:p.Glu272Ter
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ENST00000357749.6:c.814G>T
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ENSP00000350386.2:p.Glu272Ter
|
|
ENST00000467744.2:n.126+68625G>T
|
|
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NM_000390.2:c.814G>T , LRG_699t1:c.814G>T
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NP_000381.1:p.Glu272Ter
|
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XM_006724615.2:c.751G>T
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XP_006724678.1:p.Glu251Ter
|
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XM_011530839.1:c.370G>T
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XP_011529141.1:p.Glu124Ter
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NM_000390.3:c.814G>T
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NP_000381.1:p.Glu272Ter
|
|
NM_001320959.1:c.370G>T
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NP_001307888.1:p.Glu124Ter
|
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NM_001362517.1:c.370G>T
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NP_001349446.1:p.Glu124Ter
|
|
NM_001362518.1:c.370G>T
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NP_001349447.1:p.Glu124Ter
|
|
NM_001362519.1:c.370G>T
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NP_001349448.1:p.Glu124Ter
|
|
XM_017029242.2:c.814G>T
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XP_016884731.1:p.Glu272Ter
|
|
XM_017029246.1:c.370G>T
|
XP_016884735.1:p.Glu124Ter
|
|
XM_024452331.1:c.370G>T
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XP_024308099.1:p.Glu124Ter
|
|
NM_000390.4:c.814G>T
MANE Select
|
NP_000381.1:p.Glu272Ter
|
|
NM_001362518.2:c.370G>T
|
NP_001349447.1:p.Glu124Ter
|
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