ENST00000227266.10:c.477T>A
MANE Select
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ENSP00000227266.4:p.Ser159=
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|
ENST00000527018.6:c.477T>A
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ENSP00000432556.2:p.Ser159=
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ENST00000533897.2:n.525T>A
|
|
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ENST00000676612.1:c.*284T>A
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ENSP00000504440.1:n.*284T>A
|
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ENST00000677208.1:c.319-3078T>A
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ENSP00000504347.1:n.319-3078T>A
|
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ENST00000677661.1:c.*154T>A
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ENSP00000503323.1:n.*154T>A
|
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ENST00000677802.1:c.*154T>A
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ENSP00000504115.1:n.*154T>A
|
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ENST00000678395.1:c.423+54T>A
|
ENSP00000503123.1:n.423+54T>A
|
|
ENST00000678464.1:c.477T>A
|
ENSP00000503046.1:p.Ser159=
|
|
ENST00000678506.1:c.446+31T>A
|
ENSP00000503580.1:n.446+31T>A
|
|
ENST00000678520.1:c.*284T>A
|
ENSP00000503361.1:n.*284T>A
|
|
ENST00000678554.1:c.477T>A
|
ENSP00000504541.1:p.Ser159=
|
|
ENST00000678915.1:c.477T>A
|
ENSP00000504805.1:p.Ser159=
|
|
ENST00000679224.1:c.114T>A
|
ENSP00000504475.1:p.Ser38=
|
|
ENST00000227266.9:c.477T>A
|
ENSP00000227266.4:p.Ser159=
|
|
ENST00000527018.5:c.347T>A
|
|
|
ENST00000533865.5:n.499T>A
|
|
|
NM_001814.4:c.477T>A , LRG_50t1:c.477T>A
|
NP_001805.3:p.Ser159=
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|
NM_001814.5:c.477T>A
|
NP_001805.3:p.Ser159=
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|
NM_001814.6:c.477T>A
MANE Select
|
NP_001805.4:p.Ser159=
|
|