ENST00000651671.1:c.6563G>C
MANE Select
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ENSP00000498587.1:p.Gly2188Ala
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ENST00000679595.1:c.*1603G>C
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ENSP00000506241.1:n.*1603G>C
|
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ENST00000679969.1:n.3159G>C
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ENST00000680003.1:n.2895G>C
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ENST00000680133.1:c.6449G>C
|
ENSP00000505319.1:p.Gly2150Ala
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ENST00000680218.1:c.6443G>C
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ENSP00000505339.1:p.Gly2148Ala
|
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ENST00000680668.1:c.6449G>C
|
ENSP00000506336.1:p.Gly2150Ala
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ENST00000680778.1:c.4160G>C
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ENSP00000506033.1:p.Gly1387Ala
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ENST00000680924.1:c.*3963G>C
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ENSP00000506031.1:n.*3963G>C
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ENST00000681135.1:c.*4172G>C
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ENSP00000506636.1:n.*4172G>C
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ENST00000681298.1:n.4668G>C
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ENST00000681454.1:c.*5799G>C
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ENSP00000505763.1:n.*5799G>C
|
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ENST00000277541.6:c.6563G>C
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ENSP00000277541.6:p.Gly2188Ala
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NM_017617.3:c.6563G>C
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NP_060087.3:p.Gly2188Ala
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XM_011518717.1:c.5864G>C
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XP_011517019.1:p.Gly1955Ala
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NM_017617.5:c.6563G>C
MANE Select
|
NP_060087.3:p.Gly2188Ala
|
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XM_011518717.2:c.5840G>C
|
XP_011517019.2:p.Gly1947Ala
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