ENST00000389048.8:c.3539T>C
MANE Select
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ENSP00000373700.3:p.Val1180Ala
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ENST00000431873.6:c.766T>C
|
|
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ENST00000638605.1:n.416T>C
|
|
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ENST00000642122.1:c.335T>C
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ENSP00000493203.1:p.Val112Ala
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ENST00000389048.7:c.3539T>C
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ENSP00000373700.3:p.Val1180Ala
|
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ENST00000431873.5:c.419T>C
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ENSP00000414027.2:p.Val140Ala
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ENST00000618119.4:c.2408T>C
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ENSP00000482733.1:p.Val803Ala
|
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NM_004304.4:c.3539T>C
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NP_004295.2:p.Val1180Ala
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NM_001353765.1:c.335T>C
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NP_001340694.1:p.Val112Ala
|
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XM_024452778.1:c.692T>C
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XP_024308546.1:p.Val231Ala
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XM_024452779.1:c.335T>C
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XP_024308547.1:p.Val112Ala
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NM_004304.5:c.3539T>C
MANE Select
|
NP_004295.2:p.Val1180Ala
|
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NM_001353765.2:c.335T>C
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NP_001340694.1:p.Val112Ala
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