ENST00000478003.2:n.1872T>G
|
|
|
ENST00000682276.1:n.1489T>G
|
|
|
ENST00000682892.1:c.1591T>G
|
ENSP00000507214.1:p.Trp531Gly
|
|
ENST00000682952.1:n.1683T>G
|
|
|
ENST00000684455.1:c.1257T>G
|
|
|
ENST00000684642.1:c.1441T>G
|
ENSP00000507355.1:p.Trp481Gly
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ENST00000684740.1:n.2222T>G
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|
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ENST00000303236.9:c.2044T>G
MANE Select
|
ENSP00000307235.3:p.Trp682Gly
|
|
ENST00000652099.1:c.2238T>G
|
|
|
ENST00000652736.1:n.1920T>G
|
|
|
ENST00000303236.7:c.2044T>G
|
ENSP00000307235.3:p.Trp682Gly
|
|
ENST00000415570.1:c.1681T>G
|
ENSP00000412076.1:p.Trp561Gly
|
|
ENST00000419748.5:c.1591T>G
|
ENSP00000408325.1:p.Trp531Gly
|
|
ENST00000478003.1:n.610T>G
|
|
|
NM_001313915.1:c.1591T>G
|
NP_001300844.1:p.Trp531Gly
|
|
NM_004836.5:c.2044T>G
|
NP_004827.4:p.Trp682Gly
|
|
NM_004836.6:c.2044T>G
|
NP_004827.4:p.Trp682Gly
|
|
NR_110236.1:n.1576A>C
|
|
|
XM_005264649.3:c.1360T>G
|
XP_005264706.1:p.Trp454Gly
|
|
XR_939749.1:n.2323T>G
|
|
|
XM_017005376.2:c.1360T>G
|
XP_016860865.1:p.Trp454Gly
|
|
NM_004836.7:c.2044T>G
MANE Select
|
NP_004827.4:p.Trp682Gly
|
|
NM_001313915.2:c.1591T>G
|
NP_001300844.1:p.Trp531Gly
|
|