ENST00000333213.11:c.980T>G
MANE Select
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ENSP00000327487.6:p.Val327Gly
|
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ENST00000434205.8:c.677T>G
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ENSP00000406559.4:p.Val226Gly
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ENST00000545228.3:c.980T>G
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ENSP00000438169.3:p.Val327Gly
|
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ENST00000579449.2:n.779T>G
|
|
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ENST00000580013.6:n.1183T>G
|
|
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ENST00000679370.1:n.1561T>G
|
|
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ENST00000679429.1:c.*438T>G
|
ENSP00000505403.1:n.*438T>G
|
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ENST00000679443.1:n.1049T>G
|
|
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ENST00000679782.1:c.980T>G
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ENSP00000505995.1:p.Val327Gly
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ENST00000679919.1:n.1049T>G
|
|
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ENST00000679928.1:c.*591T>G
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ENSP00000506071.1:n.*591T>G
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ENST00000680528.1:n.1005T>G
|
|
|
ENST00000680999.1:c.980T>G
|
ENSP00000504984.1:p.Val327Gly
|
|
ENST00000681282.1:c.*226T>G
|
ENSP00000506339.1:n.*226T>G
|
|
ENST00000333213.10:c.980T>G
|
ENSP00000327487.6:p.Val327Gly
|
|
ENST00000545228.2:c.69T>G
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|
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ENST00000578415.1:c.940T>G
|
|
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ENST00000583173.5:c.513T>G
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ENSP00000463619.1:p.Arg171=
|
|
NM_207346.2:c.980T>G
|
NP_997229.2:p.Val327Gly
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|
XM_005257229.2:c.980T>G
|
XP_005257286.1:p.Val327Gly
|
|
XM_006721821.2:c.677T>G
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XP_006721884.1:p.Val226Gly
|
|
XM_011524616.1:c.980T>G
|
XP_011522918.1:p.Val327Gly
|
|
XM_011524617.1:c.980T>G
|
XP_011522919.1:p.Val327Gly
|
|
XM_011524618.1:c.980T>G
|
XP_011522920.1:p.Val327Gly
|
|
XR_243646.2:n.1010T>G
|
|
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XM_005257229.4:c.980T>G
|
XP_005257286.1:p.Val327Gly
|
|
XR_243646.4:n.1016T>G
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|
|
NM_207346.3:c.980T>G
MANE Select
|
NP_997229.2:p.Val327Gly
|
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