ENST00000262493.12:c.738G>T
MANE Select
|
ENSP00000262493.6:p.Glu246Asp
|
|
ENST00000562316.6:c.405G>T
|
ENSP00000457238.2:p.Glu135Asp
|
|
ENST00000564727.2:c.42G>T
|
ENSP00000454971.2:p.Glu14Asp
|
|
ENST00000568375.2:c.116-3468G>T
|
|
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ENST00000638185.1:n.953G>T
|
|
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ENST00000638210.1:n.1038G>T
|
|
|
ENST00000638705.1:c.738G>T
|
ENSP00000491223.1:p.Glu246Asp
|
|
ENST00000638836.1:n.648G>T
|
|
|
ENST00000639055.1:n.1459G>T
|
|
|
ENST00000639251.1:n.639G>T
|
|
|
ENST00000639268.1:c.373G>T
|
|
|
ENST00000639341.1:c.263G>T
|
|
|
ENST00000639770.1:c.776G>T
|
ENSP00000491999.1:n.776G>T
|
|
ENST00000640390.1:n.668G>T
|
|
|
ENST00000640469.1:c.102G>T
|
ENSP00000491875.1:p.Glu34Asp
|
|
ENST00000640560.1:n.514G>T
|
|
|
ENST00000640893.1:c.*136G>T
|
ENSP00000492677.1:n.*136G>T
|
|
ENST00000262493.10:c.738G>T
|
ENSP00000262493.6:p.Glu246Asp
|
|
ENST00000568375.1:n.116-3468G>T
|
|
|
NM_020988.2:c.738G>T
|
NP_066268.1:p.Glu246Asp
|
|
XM_011523003.1:c.612G>T
|
XP_011521305.1:p.Glu204Asp
|
|
XM_011523003.3:c.612G>T
|
XP_011521305.1:p.Glu204Asp
|
|
NM_020988.3:c.738G>T
MANE Select
|
NP_066268.1:p.Glu246Asp
|
|