ENST00000379370.7:c.3656T>G
MANE Select
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ENSP00000368678.2:p.Val1219Gly
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ENST00000651234.1:c.3341T>G
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ENSP00000499046.1:p.Val1114Gly
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|
ENST00000652369.1:c.3341T>G
|
ENSP00000498543.1:p.Val1114Gly
|
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ENST00000379370.6:c.3656T>G
|
ENSP00000368678.2:p.Val1219Gly
|
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ENST00000466223.1:n.394T>G
|
|
|
ENST00000478677.1:n.238T>G
|
|
|
ENST00000620552.4:c.3242T>G
|
ENSP00000484607.1:p.Val1081Gly
|
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NM_001305275.1:c.3656T>G
|
NP_001292204.1:p.Val1219Gly
|
|
NM_198576.3:c.3656T>G
|
NP_940978.2:p.Val1219Gly
|
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XM_005244749.2:c.3656T>G
|
XP_005244806.1:p.Val1219Gly
|
|
XM_006710635.2:c.3656T>G
|
XP_006710698.1:p.Val1219Gly
|
|
XM_011541429.1:c.3656T>G
|
XP_011539731.1:p.Val1219Gly
|
|
XM_011541430.1:c.2783T>G
|
XP_011539732.1:p.Val928Gly
|
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XM_011541431.1:c.1922T>G
|
XP_011539733.1:p.Val641Gly
|
|
XR_946650.1:n.3723T>G
|
|
|
NM_001364727.1:c.3341T>G
|
NP_001351656.1:p.Val1114Gly
|
|
XM_005244749.3:c.3656T>G
|
XP_005244806.1:p.Val1219Gly
|
|
XM_011541429.2:c.3656T>G
|
XP_011539731.1:p.Val1219Gly
|
|
XR_946650.2:n.3727T>G
|
|
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NM_001305275.2:c.3656T>G
|
NP_001292204.1:p.Val1219Gly
|
|
NM_198576.4:c.3656T>G
MANE Select
|
NP_940978.2:p.Val1219Gly
|
|
NM_001364727.2:c.3341T>G
|
NP_001351656.1:p.Val1114Gly
|
|