ENST00000388996.10:c.857T>C
MANE Select
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ENSP00000373648.3:p.Val286Ala
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ENST00000521134.6:c.497T>C
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ENSP00000429799.1:p.Val166Ala
|
|
ENST00000638588.1:c.530T>C
|
ENSP00000491940.1:p.Val177Ala
|
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ENST00000639358.1:c.507T>C
|
|
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ENST00000639496.1:c.530T>C
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ENSP00000491165.1:p.Val177Ala
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ENST00000388996.8:c.857T>C
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ENSP00000373648.3:p.Val286Ala
|
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ENST00000519445.5:c.857T>C
|
ENSP00000428790.1:p.Val286Ala
|
|
ENST00000519589.1:n.635T>C
|
|
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ENST00000521134.5:c.497T>C
|
ENSP00000429799.1:p.Val166Ala
|
|
ENST00000621976.1:c.494T>C
|
ENSP00000482510.1:p.Val165Ala
|
|
NM_001204824.1:c.497T>C
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NP_001191753.1:p.Val166Ala
|
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NM_004519.3:c.857T>C
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NP_004510.1:p.Val286Ala
|
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XM_005250914.2:c.-300T>C
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XP_005250971.1:n.-300T>C
|
|
XM_006716555.2:c.149T>C
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XP_006716618.1:p.Val50Ala
|
|
XM_011517026.1:c.497T>C
|
XP_011515328.1:p.Val166Ala
|
|
XM_005250914.3:c.-300T>C
|
XP_005250971.1:n.-300T>C
|
|
XM_006716555.3:c.149T>C
|
XP_006716618.1:p.Val50Ala
|
|
XM_011517026.2:c.497T>C
|
XP_011515328.1:p.Val166Ala
|
|
XM_017013400.1:c.635T>C
|
XP_016868889.1:p.Val212Ala
|
|
NM_004519.4:c.857T>C
MANE Select
|
NP_004510.1:p.Val286Ala
|
|
NM_001204824.2:c.497T>C
|
NP_001191753.1:p.Val166Ala
|
|