|
ENST00000261769.10:c.2425A>T
MANE Select
|
ENSP00000261769.4:p.Asn809Tyr
|
|
|
ENST00000261769.9:c.2425A>T
|
ENSP00000261769.4:p.Asn809Tyr
|
|
|
ENST00000422392.6:c.2242A>T
|
ENSP00000414946.2:p.Asn748Tyr
|
|
|
ENST00000562118.1:n.643A>T
|
|
|
|
ENST00000562836.5:n.2496A>T
|
|
|
|
ENST00000566510.5:c.*1091A>T
|
ENSP00000458139.1:n.*1091A>T
|
|
|
ENST00000566612.5:c.*665A>T
|
ENSP00000454782.1:n.*665A>T
|
|
|
ENST00000611625.4:c.2488A>T
|
ENSP00000481063.1:p.Asn830Tyr
|
|
|
ENST00000612417.4:c.1853+3229A>T
|
ENSP00000478360.1:n.1853+3229A>T
|
|
|
ENST00000621016.4:c.1866-4420A>T
|
ENSP00000480664.1:n.1866-4420A>T
|
|
|
NM_004360.3:c.2425A>T , LRG_301t1:c.2425A>T
|
NP_004351.1:p.Asn809Tyr
|
|
|
XM_011523488.1:c.1690A>T
|
XP_011521790.1:p.Asn564Tyr
|
|
|
XM_011523489.1:c.1690A>T
|
XP_011521791.1:p.Asn564Tyr
|
|
|
NM_001317184.1:c.2242A>T
|
NP_001304113.1:p.Asn748Tyr
|
|
|
NM_001317185.1:c.877A>T
|
NP_001304114.1:p.Asn293Tyr
|
|
|
NM_001317186.1:c.460A>T
|
NP_001304115.1:p.Asn154Tyr
|
|
|
NM_004360.4:c.2425A>T
|
NP_004351.1:p.Asn809Tyr
|
|
|
NM_004360.5:c.2425A>T
MANE Select
|
NP_004351.1:p.Asn809Tyr
|
|
|
NM_001317184.2:c.2242A>T
|
NP_001304113.1:p.Asn748Tyr
|
|
|
NM_001317185.2:c.877A>T
|
NP_001304114.1:p.Asn293Tyr
|
|
|
NM_001317186.2:c.460A>T
|
NP_001304115.1:p.Asn154Tyr
|
|
