ENST00000299506.3:c.212T>C
MANE Select
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ENSP00000299506.3:p.Val71Ala
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ENST00000299506.2:c.212T>C
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ENSP00000299506.2:p.Val71Ala
|
|
ENST00000305253.8:c.377T>C
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ENSP00000305426.4:p.Val126Ala
|
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ENST00000534099.5:c.230T>C
|
ENSP00000434400.1:p.Val77Ala
|
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NM_003320.4:c.377T>C
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NP_003311.2:p.Val126Ala
|
|
NM_177972.2:c.212T>C
|
NP_813977.1:p.Val71Ala
|
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XM_005253109.2:c.338T>C
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XP_005253166.1:p.Val113Ala
|
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XM_011520344.1:c.248T>C
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XP_011518646.1:p.Val83Ala
|
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XM_005253109.3:c.338T>C
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XP_005253166.1:p.Val113Ala
|
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XM_011520344.2:c.248T>C
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XP_011518646.1:p.Val83Ala
|
|
NM_177972.3:c.212T>C
MANE Select
|
NP_813977.1:p.Val71Ala
|
|
NM_003320.5:c.377T>C
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NP_003311.2:p.Val126Ala
|
|