ENST00000285398.7:c.2098G>T
MANE Select
|
ENSP00000285398.2:p.Asp700Tyr
|
|
ENST00000644317.1:c.*1587G>T
|
ENSP00000494012.1:n.*1587G>T
|
|
ENST00000645233.1:c.*2310G>T
|
ENSP00000494116.1:n.*2310G>T
|
|
ENST00000645467.1:c.*870G>T
|
ENSP00000494889.1:n.*870G>T
|
|
ENST00000645736.1:c.1769G>T
|
ENSP00000494545.1:n.1769G>T
|
|
ENST00000646042.1:n.2833G>T
|
|
|
ENST00000646654.1:c.*1565G>T
|
ENSP00000494526.1:n.*1565G>T
|
|
ENST00000647169.1:c.2173G>T
|
ENSP00000495619.1:p.Asp725Tyr
|
|
ENST00000647496.1:c.396-1813G>T
|
|
|
ENST00000285398.6:c.2098G>T
|
ENSP00000285398.2:p.Asp700Tyr
|
|
ENST00000426778.5:c.*2079G>T
|
ENSP00000415335.1:n.*2079G>T
|
|
ENST00000445889.5:c.*2141G>T
|
ENSP00000390888.1:n.*2141G>T
|
|
ENST00000491292.5:n.3468G>T
|
|
|
NM_000122.1:c.2098G>T , LRG_462t1:c.2098G>T
|
NP_000113.1:p.Asp700Tyr
|
|
NM_001303416.1:c.1906G>T
|
NP_001290345.1:p.Asp636Tyr
|
|
NM_001303418.1:c.1906G>T
|
NP_001290347.1:p.Asp636Tyr
|
|
XM_011510794.1:c.2116G>T
|
XP_011509096.1:p.Asp706Tyr
|
|
XM_011510795.1:c.1660G>T
|
XP_011509097.1:p.Asp554Tyr
|
|
XM_011510794.2:c.2116G>T
|
XP_011509096.1:p.Asp706Tyr
|
|
XM_017003583.1:c.1642G>T
|
XP_016859072.1:p.Asp548Tyr
|
|
NM_000122.2:c.2098G>T
MANE Select
|
NP_000113.1:p.Asp700Tyr
|
|
NM_001303416.2:c.1906G>T
|
NP_001290345.1:p.Asp636Tyr
|
|
NM_001303418.2:c.1906G>T
|
NP_001290347.1:p.Asp636Tyr
|
|