ENST00000307050.6:c.-99-36963T>C
MANE Select
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ENSP00000305926.5:n.-99-36963T>C
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ENST00000560598.2:c.-222-4559T>C
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ENSP00000453883.2:n.-222-4559T>C
|
|
ENST00000558371.5:n.73-4559T>C
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|
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ENST00000560536.5:c.-222-4559T>C
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ENSP00000453622.1:n.-222-4559T>C
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ENST00000560598.1:c.-222-4559T>C
|
ENSP00000453883.1:n.-222-4559T>C
|
|
XM_011521287.1:c.-201-4559T>C
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XP_011519589.1:n.-201-4559T>C
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NM_001329907.1:c.-222-4559T>C
|
NP_001316836.1:n.-222-4559T>C
|
|
NM_130901.2:c.-222-4559T>C
|
NP_570971.1:n.-222-4559T>C
|
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NM_001329907.2:c.-222-4559T>C
|
NP_001316836.1:n.-222-4559T>C
|
|
NM_130901.3:c.-222-4559T>C
|
NP_570971.1:n.-222-4559T>C
|
|
NM_001382637.1:c.-99-36963T>C
MANE Select
|
NP_001369566.1:n.-99-36963T>C
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