ENST00000252029.8:c.294G>T
MANE Select
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ENSP00000252029.3:p.Ser98=
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ENST00000395680.6:c.294G>T
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ENSP00000379037.1:p.Ser98=
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ENST00000395681.6:c.294G>T
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ENSP00000379038.1:p.Ser98=
|
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ENST00000650719.1:c.294G>T
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ENSP00000498276.1:p.Ser98=
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ENST00000651095.1:n.433G>T
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|
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ENST00000651196.1:c.294G>T
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ENSP00000499096.1:p.Ser98=
|
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ENST00000651401.1:c.-1+645G>T
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ENSP00000499115.1:n.-1+645G>T
|
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ENST00000651906.1:n.413G>T
|
|
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ENST00000652237.1:n.570G>T
|
|
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ENST00000652352.1:c.42G>T
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ENSP00000498579.1:p.Ser14=
|
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ENST00000252029.7:c.294G>T
|
ENSP00000252029.3:p.Ser98=
|
|
ENST00000395678.7:c.294G>T
|
ENSP00000379036.3:p.Ser98=
|
|
ENST00000395680.5:c.294G>T
|
ENSP00000379037.1:p.Ser98=
|
|
ENST00000395681.5:c.294G>T
|
ENSP00000379038.1:p.Ser98=
|
|
ENST00000425169.1:c.294G>T
|
ENSP00000395875.1:p.Ser98=
|
|
ENST00000476284.1:n.419G>T
|
|
|
ENST00000487162.1:n.582G>T
|
|
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ENST00000487577.5:n.581G>T
|
|
|
NM_001113755.2:c.294G>T
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NP_001107227.1:p.Ser98=
|
|
NM_001113756.2:c.294G>T
|
NP_001107228.1:p.Ser98=
|
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NM_001257988.1:c.294G>T , LRG_727t1:c.294G>T
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NP_001244917.1:p.Ser98=
|
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NM_001257989.1:c.294G>T , LRG_727t2:c.294G>T
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NP_001244918.1:p.Ser98=
|
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NM_001953.4:c.294G>T
|
NP_001944.1:p.Ser98=
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|
NM_001113755.3:c.294G>T
|
NP_001107227.1:p.Ser98=
|
|
NM_001113756.3:c.294G>T
|
NP_001107228.1:p.Ser98=
|
|
NM_001953.5:c.294G>T
MANE Select
|
NP_001944.1:p.Ser98=
|
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