ENST00000262493.12:c.819T>A
MANE Select
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ENSP00000262493.6:p.Asp273Glu
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ENST00000562316.6:c.486T>A
|
ENSP00000457238.2:p.Asp162Glu
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|
ENST00000564727.2:c.123T>A
|
ENSP00000454971.2:p.Asp41Glu
|
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ENST00000568375.2:c.116-3387T>A
|
|
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ENST00000638185.1:n.1034T>A
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|
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ENST00000638210.1:n.1119T>A
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|
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ENST00000638705.1:c.819T>A
|
ENSP00000491223.1:p.Asp273Glu
|
|
ENST00000638836.1:n.729T>A
|
|
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ENST00000639055.1:n.1540T>A
|
|
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ENST00000639251.1:n.720T>A
|
|
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ENST00000639268.1:c.454T>A
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|
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ENST00000639341.1:c.344T>A
|
|
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ENST00000639770.1:c.857T>A
|
ENSP00000491999.1:n.857T>A
|
|
ENST00000640390.1:n.749T>A
|
|
|
ENST00000640469.1:c.183T>A
|
ENSP00000491875.1:p.Asp61Glu
|
|
ENST00000640560.1:n.595T>A
|
|
|
ENST00000640893.1:c.*217T>A
|
ENSP00000492677.1:n.*217T>A
|
|
ENST00000262493.10:c.819T>A
|
ENSP00000262493.6:p.Asp273Glu
|
|
ENST00000564727.1:c.39T>A
|
ENSP00000454971.1:p.Asp13Glu
|
|
ENST00000568375.1:n.116-3387T>A
|
|
|
NM_020988.2:c.819T>A
|
NP_066268.1:p.Asp273Glu
|
|
XM_011523003.1:c.693T>A
|
XP_011521305.1:p.Asp231Glu
|
|
XM_011523003.3:c.693T>A
|
XP_011521305.1:p.Asp231Glu
|
|
NM_020988.3:c.819T>A
MANE Select
|
NP_066268.1:p.Asp273Glu
|
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