ENST00000622290.5:c.*290C=
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ENSP00000483331.2:n.*290C=
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ENST00000205557.12:c.4118C=
MANE Select
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ENSP00000205557.7:p.Ala1373=
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ENST00000640696.1:c.932C=
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ENSP00000492197.1:p.Ala311=
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ENST00000205557.11:c.4118C=
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ENSP00000205557.7:p.Ala1373=
|
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ENST00000456970.6:c.3743C=
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ENSP00000405002.2:n.3743C=
|
|
ENST00000576204.5:n.981C=
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|
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ENST00000622290.4:c.*1327C=
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ENSP00000483331.1:n.*1327C=
|
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NM_001171.5:c.4118C=
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NP_001162.4:p.Ala1373=
|
|
XM_011522479.1:c.4085C=
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XP_011520781.1:p.Ala1362=
|
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XM_011522480.1:c.3776C=
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XP_011520782.1:p.Ala1259=
|
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XM_011522481.1:c.3776C=
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XP_011520783.1:p.Ala1259=
|
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XR_933134.1:n.539-5063G=
|
|
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NM_001351800.1:c.3776C=
|
NP_001338729.1:p.Ala1259=
|
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NR_147784.1:n.3780C=
|
|
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XM_011522479.2:c.4085C=
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XP_011520781.1:p.Ala1362=
|
|
XM_011522481.3:c.3776C=
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XP_011520783.1:p.Ala1259=
|
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XM_017023212.1:c.3950C=
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XP_016878701.1:p.Ala1317=
|
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XM_024450261.1:c.4154C=
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XP_024306029.1:p.Ala1385=
|
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NM_001171.6:c.4118C=
MANE Select
|
NP_001162.5:p.Ala1373=
|
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