ENST00000350721.9:c.6545T>A
MANE Select
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ENSP00000343741.4:p.Val2182Glu
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ENST00000513291.2:n.1729T>A
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ENST00000654170.1:n.1388T>A
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|
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ENST00000656590.1:c.5335T>A
|
|
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ENST00000661310.1:c.6353T>A
|
ENSP00000499589.1:p.Val2118Glu
|
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ENST00000665483.1:n.400T>A
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ENST00000666447.1:n.380T>A
|
|
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ENST00000666943.1:n.2009T>A
|
|
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ENST00000350721.8:c.6545T>A
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ENSP00000343741.4:p.Val2182Glu
|
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ENST00000513291.1:c.84T>A
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NM_001184.3:c.6545T>A
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NP_001175.2:p.Val2182Glu
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XM_011512924.1:c.6551T>A
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XP_011511226.1:p.Val2184Glu
|
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XM_011512925.1:c.6359T>A
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XP_011511227.1:p.Val2120Glu
|
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XR_924147.1:n.6640T>A
|
|
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XR_924148.1:n.6640T>A
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|
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XR_924149.1:n.6519T>A
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|
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NM_001354579.1:c.6353T>A
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NP_001341508.1:p.Val2118Glu
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XR_001740179.2:n.6634T>A
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|
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XR_924148.2:n.6640T>A
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|
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NM_001184.4:c.6545T>A
MANE Select
|
NP_001175.2:p.Val2182Glu
|
|
NM_001354579.2:c.6353T>A
|
NP_001341508.1:p.Val2118Glu
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