ENST00000262493.12:c.785A>T
MANE Select
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ENSP00000262493.6:p.Asp262Val
|
|
ENST00000562316.6:c.452A>T
|
ENSP00000457238.2:p.Asp151Val
|
|
ENST00000564727.2:c.89A>T
|
ENSP00000454971.2:p.Asp30Val
|
|
ENST00000568375.2:c.116-3421A>T
|
|
|
ENST00000638185.1:n.1000A>T
|
|
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ENST00000638210.1:n.1085A>T
|
|
|
ENST00000638705.1:c.785A>T
|
ENSP00000491223.1:p.Asp262Val
|
|
ENST00000638836.1:n.695A>T
|
|
|
ENST00000639055.1:n.1506A>T
|
|
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ENST00000639251.1:n.686A>T
|
|
|
ENST00000639268.1:c.420A>T
|
|
|
ENST00000639341.1:c.310A>T
|
|
|
ENST00000639770.1:c.823A>T
|
ENSP00000491999.1:n.823A>T
|
|
ENST00000640390.1:n.715A>T
|
|
|
ENST00000640469.1:c.149A>T
|
ENSP00000491875.1:p.Asp50Val
|
|
ENST00000640560.1:n.561A>T
|
|
|
ENST00000640893.1:c.*183A>T
|
ENSP00000492677.1:n.*183A>T
|
|
ENST00000262493.10:c.785A>T
|
ENSP00000262493.6:p.Asp262Val
|
|
ENST00000564727.1:c.5A>T
|
ENSP00000454971.1:p.Asp2Val
|
|
ENST00000568375.1:n.116-3421A>T
|
|
|
NM_020988.2:c.785A>T
|
NP_066268.1:p.Asp262Val
|
|
XM_011523003.1:c.659A>T
|
XP_011521305.1:p.Asp220Val
|
|
XM_011523003.3:c.659A>T
|
XP_011521305.1:p.Asp220Val
|
|
NM_020988.3:c.785A>T
MANE Select
|
NP_066268.1:p.Asp262Val
|
|