ENST00000350721.9:c.6292G>T
MANE Select
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ENSP00000343741.4:p.Gly2098Cys
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ENST00000513291.2:n.1476G>T
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ENST00000654170.1:n.1135G>T
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|
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ENST00000656590.1:c.5082G>T
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|
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ENST00000661310.1:c.6100G>T
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ENSP00000499589.1:p.Gly2034Cys
|
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ENST00000665483.1:n.147G>T
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ENST00000666447.1:n.127G>T
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|
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ENST00000666943.1:n.1756G>T
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|
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ENST00000350721.8:c.6292G>T
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ENSP00000343741.4:p.Gly2098Cys
|
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NM_001184.3:c.6292G>T
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NP_001175.2:p.Gly2098Cys
|
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XM_011512924.1:c.6298G>T
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XP_011511226.1:p.Gly2100Cys
|
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XM_011512925.1:c.6106G>T
|
XP_011511227.1:p.Gly2036Cys
|
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XR_924147.1:n.6387G>T
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XR_924148.1:n.6387G>T
|
|
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XR_924149.1:n.6266G>T
|
|
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NM_001354579.1:c.6100G>T
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NP_001341508.1:p.Gly2034Cys
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XR_001740179.2:n.6381G>T
|
|
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XR_001740180.2:n.6435G>T
|
|
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XR_001740181.2:n.6314G>T
|
|
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XR_001740182.1:n.6266G>T
|
|
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XR_002959543.1:n.6491G>T
|
|
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XR_924148.2:n.6387G>T
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|
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NM_001184.4:c.6292G>T
MANE Select
|
NP_001175.2:p.Gly2098Cys
|
|
NM_001354579.2:c.6100G>T
|
NP_001341508.1:p.Gly2034Cys
|
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