ENST00000298910.12:c.6082G>T
MANE Select
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ENSP00000298910.7:p.Gly2028Trp
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ENST00000679360.1:c.*4991G>T
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ENSP00000505368.1:n.*4991G>T
|
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ENST00000679532.1:c.1856G>T
|
|
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ENST00000680018.1:c.1527G>T
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ENSP00000505347.1:n.1527G>T
|
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ENST00000680422.1:c.1727G>T
|
|
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ENST00000680425.1:c.1249G>T
|
ENSP00000506459.1:n.1249G>T
|
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ENST00000680453.1:c.1539G>T
|
|
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ENST00000680790.1:c.5827G>T
|
ENSP00000505335.1:p.Gly1943Trp
|
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ENST00000681136.1:n.2066G>T
|
|
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ENST00000681696.1:c.1765G>T
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ENSP00000505871.1:p.Gly589Trp
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ENST00000298910.11:c.6082G>T
|
ENSP00000298910.7:p.Gly2028Trp
|
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ENST00000430804.5:c.3378G>T
|
|
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ENST00000479187.5:n.2763G>T
|
|
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NM_198578.3:c.6082G>T
|
NP_940980.3:p.Gly2028Trp
|
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XM_005268629.2:c.6082G>T
|
XP_005268686.1:p.Gly2028Trp
|
|
XM_011537877.1:c.6082G>T
|
XP_011536179.1:p.Gly2028Trp
|
|
XM_011537878.1:c.6082G>T
|
XP_011536180.1:p.Gly2028Trp
|
|
XM_011537879.1:c.4879G>T
|
XP_011536181.1:p.Gly1627Trp
|
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XM_005268629.4:c.6082G>T
|
XP_005268686.1:p.Gly2028Trp
|
|
XM_011537877.3:c.6082G>T
|
XP_011536179.1:p.Gly2028Trp
|
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XM_017018787.1:c.2998G>T
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XP_016874276.1:p.Gly1000Trp
|
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XM_017018788.2:c.2344G>T
|
XP_016874277.1:p.Gly782Trp
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|
XM_024448833.1:c.4879G>T
|
XP_024304601.1:p.Gly1627Trp
|
|
NM_198578.4:c.6082G>T
MANE Select
|
NP_940980.4:p.Gly2028Trp
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