ENST00000331222.6:c.585G>T
MANE Select
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ENSP00000328182.4:p.Trp195Cys
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ENST00000519254.2:c.585G>T
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ENSP00000490016.1:p.Trp195Cys
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|
ENST00000520991.3:c.647G>T
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ENSP00000487905.2:p.Gly216Val
|
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ENST00000635751.1:c.585G>T
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ENSP00000489694.1:p.Trp195Cys
|
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ENST00000635773.1:c.496+8694G>T
|
|
|
ENST00000635855.1:c.543+8694G>T
|
ENSP00000489726.1:n.543+8694G>T
|
|
ENST00000635970.1:c.585G>T
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ENSP00000490439.1:p.Trp195Cys
|
|
ENST00000636175.1:c.343+8694G>T
|
|
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ENST00000636934.1:c.543+8694G>T
|
ENSP00000490218.1:n.543+8694G>T
|
|
ENST00000637083.1:c.585G>T
|
ENSP00000490235.1:p.Trp195Cys
|
|
ENST00000637156.1:c.585G>T
|
ENSP00000490458.1:p.Trp195Cys
|
|
ENST00000331222.4:c.585G>T
|
ENSP00000328182.4:p.Trp195Cys
|
|
ENST00000519254.1:n.104G>T
|
|
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ENST00000523237.1:n.360G>T
|
|
|
NM_018941.3:c.585G>T , LRG_691t1:c.585G>T
|
NP_061764.2:p.Trp195Cys
|
|
XM_005266021.3:c.585G>T
|
XP_005266078.1:p.Trp195Cys
|
|
XM_005266022.1:c.585G>T
|
XP_005266079.1:p.Trp195Cys
|
|
XM_005266023.1:c.585G>T
|
XP_005266080.1:p.Trp195Cys
|
|
XM_011534745.1:c.585G>T
|
XP_011533047.1:p.Trp195Cys
|
|
XM_011534746.1:c.585G>T
|
XP_011533048.1:p.Trp195Cys
|
|
XM_005266021.4:c.585G>T
|
XP_005266078.1:p.Trp195Cys
|
|
XM_011534746.2:c.585G>T
|
XP_011533048.1:p.Trp195Cys
|
|
NM_018941.4:c.585G>T
MANE Select
|
NP_061764.2:p.Trp195Cys
|
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