ENST00000252029.8:c.922A=
MANE Select
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ENSP00000252029.3:p.Thr308=
|
|
ENST00000395680.6:c.922A=
|
ENSP00000379037.1:p.Thr308=
|
|
ENST00000395681.6:c.922A=
|
ENSP00000379038.1:p.Thr308=
|
|
ENST00000650719.1:c.803A=
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ENSP00000498276.1:p.His268=
|
|
ENST00000651401.1:c.406A=
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ENSP00000499115.1:p.Thr136=
|
|
ENST00000652401.1:c.423A=
|
|
|
ENST00000252029.7:c.922A=
|
ENSP00000252029.3:p.Thr308=
|
|
ENST00000395678.7:c.922A=
|
ENSP00000379036.3:p.Thr308=
|
|
ENST00000395680.5:c.922A=
|
ENSP00000379037.1:p.Thr308=
|
|
ENST00000395681.5:c.922A=
|
ENSP00000379038.1:p.Thr308=
|
|
ENST00000425169.1:c.823A=
|
ENSP00000395875.1:p.Thr275=
|
|
ENST00000476284.1:n.928A=
|
|
|
ENST00000487577.5:n.1209A=
|
|
|
NM_001113755.2:c.922A=
|
NP_001107227.1:p.Thr308=
|
|
NM_001113756.2:c.922A=
|
NP_001107228.1:p.Thr308=
|
|
NM_001257988.1:c.922A= , LRG_727t1:c.922A=
|
NP_001244917.1:p.Thr308=
|
|
NM_001257989.1:c.922A= , LRG_727t2:c.922A=
|
NP_001244918.1:p.Thr308=
|
|
NM_001953.4:c.922A=
|
NP_001944.1:p.Thr308=
|
|
NM_001113755.3:c.922A=
|
NP_001107227.1:p.Thr308=
|
|
NM_001113756.3:c.922A=
|
NP_001107228.1:p.Thr308=
|
|
NM_001953.5:c.922A=
MANE Select
|
NP_001944.1:p.Thr308=
|
|