ENST00000326003.7:c.493T>A
MANE Select
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ENSP00000314151.1:p.Phe165Ile
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ENST00000326003.6:c.493T>A
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ENSP00000314151.1:p.Phe165Ile
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|
ENST00000360617.7:c.493T>A
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ENSP00000353829.2:p.Phe165Ile
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ENST00000422986.6:c.*149T>A
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ENSP00000393628.2:n.*149T>A
|
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ENST00000593997.5:c.493T>A
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ENSP00000472907.1:p.Phe165Ile
|
|
ENST00000595392.5:c.369T>A
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ENSP00000468912.1:p.Ser123Arg
|
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ENST00000595952.5:c.364T>A
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ENSP00000471155.1:p.Phe122Ile
|
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ENST00000596185.5:c.*601T>A
|
ENSP00000471648.1:n.*601T>A
|
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ENST00000596333.1:n.528T>A
|
|
|
ENST00000597286.5:c.382T>A
|
ENSP00000470523.1:p.Phe128Ile
|
|
ENST00000597483.5:c.364T>A
|
ENSP00000472411.1:p.Phe122Ile
|
|
ENST00000598145.1:c.477T>A
|
|
|
ENST00000601349.5:n.1772T>A
|
|
|
ENST00000601503.5:c.436T>A
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ENSP00000472213.1:p.Phe146Ile
|
|
ENST00000601812.1:n.925T>A
|
|
|
ENST00000617027.4:c.370T>A
|
ENSP00000483513.1:p.Phe124Ile
|
|
NM_001030047.1:c.493T>A
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NP_001025218.1:p.Phe165Ile
|
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NM_001030048.1:c.364T>A
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NP_001025219.1:p.Phe122Ile
|
|
NM_001648.2:c.493T>A
MANE Select
|
NP_001639.1:p.Phe165Ile
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XM_011526923.1:c.493T>A
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XP_011525225.1:p.Cys165Ser
|
|
XM_011526924.1:c.493T>A
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XP_011525226.1:p.Cys165Ser
|
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XR_935817.1:n.528T>A
|
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